Article Text

Original research
ACTonDiabetes—a guided psychological internet intervention based on Acceptance and Commitment Therapy (ACT) for adults living with type 1 or 2 diabetes: results of a randomised controlled feasibility trial
  1. Eileen Bendig1,
  2. Natalie Bauereiss1,
  3. Andreas Schmitt2,3,
  4. Patrick Albus1,
  5. Harald Baumeister1
  1. 1Department of Clinical Psychology and Psychotherapy, Institute of Psychology and Education, Ulm University, Ulm, Germany
  2. 2Research Institute of the Diabetes Academy Mergentheim, Diabetes Academy Bad Mergentheim, Bad Mergentheim, Germany
  3. 3German Center for Diabetes Research (DZD), München-Neuherberg, Germany
  1. Correspondence to Ms Eileen Bendig; eileen.bendig{at}uni-ulm.de

Abstract

Objectives This two-group randomised controlled trial evaluates the feasibility of an Acceptance and Commitment Therapy (ACT)-based internet intervention for diabetes distress in people with diabetes type 1 or type 2. Participants were assigned to a guided self-help intervention (EG) or waitlist control group (CG).

Setting Recruitment took place following an open recruitment strategy including different diabetes centres, self-help groups and social media platforms.

Participants Eligibility criteria comprised being 18 years of age or older, self-reported diagnosis of type 1 or type 2 diabetes, internet access, sufficient German language skills and written informed consent.

Intervention ACTonDiabetes is an internet-based and mobile-based intervention and comprises an introduction and seven modules (one module per week, processing time about 45–60 min). Intervention contents are based on ACT.

Primary and secondary outcome measures Participants were assessed before and 8 weeks after randomisation. Primary outcome was feasibility (trial recruitment, acceptability). Potential group differences in diabetes distress and other outcomes at follow-up were analysed using linear regression models with baseline values as predictors. All analyses were based on an intention-to-treat principle, potential negative effects were analysed on per-protocol basis.

Results From October 2017 to April 2018, N=42 people with diabetes consented and were randomised (EG n=21, CG n=21). Forty-three per cent of the EG completed all treatment modules within 8 weeks. Across modules, formative user feedback revealed that contents could be optimised regarding comprehensibility (34%), individualisation (20%) and text amount (21%). Overall, 57% of participants dropped out prior to full treatment completion. There were reductions of diabetes distress in the EG (d=0.65, p=0.042).

Conclusions Modifications of the intervention content according to the user feedback will be performed to further improve acceptability. Mechanisms to foster intervention adherence should be considered for lowering the attrition rate. ACTonDiabetes is feasible for the implementation in a confirmatory trial.

Trial registration number WHO International Clinical Trials Registry Platform via the German Clinical Trials Register (DRKS) (DRKS00013193).

  • diabetes & endocrinology
  • depression & mood disorders
  • adult psychiatry

Data availability statement

Data are available upon reasonable request.

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Strengths and limitations of this study

  • This is the first trial on an Acceptance and Commitment Therapy-based internet intervention for people with diabetes.

  • The intervention was adapted from a previously evaluated treatment concept for people with a chronic somatic disease.

  • This feasibility trial promotes a responsible use of resources and a high standard of quality in a confirmatory trial.

  • Attrition was high in both comparison groups.

  • Formative user feedback is used to further improve the ACTonDiabetes intervention.

Introduction

The prevalence and incidence rates of diabetes are increasing worldwide.1 For Germany, there is an assumed increase of between 10.7 million (+54%) and 12.3 million (+77%) type 2 diabetes cases until 2040.2 Additionally, the rate of individual years lived with diabetes is rising globally.1 Against the background of these developments, the editorial of The Lancet speaks of a ‘diabetes pandemic’.3 Diabetes care constitutes an enormous economic burden for healthcare systems as well as an enormous burden on the level of individuals due to years lived with the disease.1 4 Living with diabetes type 1 or 2 is challenging.5 It comes along with a multitude of requirements that need to be considered and mastered in everyday life.5 Requirements comprise permanent self-treatment and monitoring,5–7 adhering to complex treatment plans,8 9 and promoting coping mechanisms to deal with diagnosis and disease.10 Consequently, the prevalence of diabetes distress is high. Diabetes distress is defined as experiencing negative emotions and burden due to the demanding and progressive conditions of living with diabetes.11 12 It involves negative emotional reactions5 such as feeling overwhelmed by the demands of living with diabetes, worries and fears about possible complications, frustration due to perceived limitations regarding lifestyle or suboptimal treatment outcomes.13 14 About 36% of people with type 212 and 41% of the people with type 1 diabetes15 report elevated diabetes distress. This has consequences in many respects.

Diabetes distress has been associated with impaired psychological well-being, reduced treatment adherence,14 reduced glycaemic control16 and common comorbid mental disorders like depression.17 In relation to this, a longitudinal study shows that diabetes distress can be associated with a higher incidence and persistence of depressive symptoms.18 Clinical treatment guidelines recommend the assessment of and interventions for reducing diabetes distress as integral part of diabetes care.19–21 However, elevated diabetes distress often remains untreated or undertreated due to various barriers.20–22 Barriers include fear of stigmatisation, limited mobility of patients, time and resources as well as limited access and availability of psychological interventions.23 24 Barriers can also arise on the part of healthcare professionals not detecting or being not able to address diabetes distress within routine consultations.25

Innovative technologies can help to overcome these barriers by delivering low-threshold digitised interventions on a large scale.26 27 In this context, internet interventions have been considered a cost-effective and flexible approach to provide psychological interventions to people with diabetes.28 29 Internet interventions are (guided) self-help programmes which can be provided on a website30 and complemented with mobile-based applications like apps.26 27 Guidance refers to human support from e-coaches (eg, psychologist/physician).30 Evidence suggests that at least a minimum of guidance can constitute an effect-facilitating factor.31 32 A recent meta-analysis investigating internet interventions for people with mental disorders and/or chronic somatic conditions suggests that guided internet interventions can be as effective as traditional face-to-face interventions.33 Internet interventions have been effectively used to support behaviour change (weight loss,34 physical activity,35 glycaemic control,36 smoking cessation,37 alcohol consumption38). Additionally, they were effectively used for treating comorbid mental disorders in people with diabetes28 39 and clinically relevant diabetes distress.28 29 Nevertheless, overall evidence in the field is still very limited with regard to quantity and quality of studies.26 To date, interventional studies have not focused on diabetes distress as primary outcome in this field of research.

Nobis et al40 evaluated a guided internet intervention for people with diabetes type 1 or 2 with depressive symptom severity as primary outcome. Authors compared the treatment group with an active control group receiving psychoeducation. On the level of secondary outcomes of this trial, results indicated a significant effect of d=0.58 (95% CI 0.33 to 0.83, p<0.001) for the reduction of diabetes distress post-treatment which persisted after 6 months (d=0.50, 95% CI 0.04 to 0.54, p<0.001).41 Likewise, van Bastelaar et al29 found significantly greater reductions of diabetes distress in the treatment group receiving internet-based depression treatment compared with a waitlist control group. The evaluated interventions were both based on cognitive–behavioural therapy (CBT).29 40

While most previously studied internet interventions are theoretically based on CBT,42 people with chronic somatic conditions might benefit from interventions that focus less on aspects of ‘change’ and more on ‘acceptance’ of the unchangeable condition as in Acceptance and Commitment-based Therapy (ACT).43 44 ACT aims at increasing psychological flexibility by fostering acceptance of unchangeable aspects in life43 44 like living with diabetes.45 Recent studies show positive effects of ACT in this population regarding self-management.45 46 Gregg et al45 as well as Shayeghian et al46 found that people receiving an ACT intervention performed better diabetes self-care and had more optimal glycated haemoglobin (HbA1c) values after the treatment than the active control group which received a structured education workshop on diabetes control. However, one study of Maghsoudi et al47 did not find significant reductions in diabetes distress following a group-based ACT intervention (eight weekly 90-minute sessions) in comparison with a treatment-as-usual control group. Further studies are being initiated recently.48

To our knowledge, this is the first study on an ACT-based internet intervention aiming at reducing elevated diabetes distress. Notably, the effectiveness and cost-effectiveness of the internet intervention ‘ACTonPain’ aiming at reducing pain-related burden in people with chronic pain were supported in studies by Lin et al.49–51 ACTonDiabetes was built on the ACTonPain treatment programme to develop a widely practicable, local and temporal flexible, low-threshold internet intervention to reduce diabetes distress in people with type 1 and type 2 diabetes.

The present study evaluates the feasibility of the programme ACTonDiabetes. Therefore, trial recruitment, acceptability and preliminary results regarding the effectiveness of the intervention are investigated. Results will inform decision processes concerning study procedures, potential amendments and the design of a future definitive trial. User feedback will be used to further improve and refine the ACTonDiabetes intervention. Specifically, this study aimed to:

  1. Explore the feasibility of trial recruitment and acceptability of the internet intervention.

  2. Examine if the intervention potentially affects diabetes distress and other intended outcomes of a future full-scale trial.

Methods

Participants

People were eligible to participate in this study if they were 18 years of age or older, had a self-reported diagnosis of type 1 or type 2 diabetes, had internet access, sufficient German language skills and provided written informed consent. Participants received the consent forms digitised or printed and were asked to sign and return them. Participants were excluded if they had other forms of diabetes (eg, gestational diabetes).

Study design and assessment

This parallel group, randomised-controlled feasibility trial enrolled participants from October 2017 to April 2018. The intervention group (EG) received the guided ACTonDiabetes intervention and was compared with a waitlist control group (CG) which started the unguided intervention 8 weeks after randomisation. This trial was conducted in accordance with the Declaration of Helsinki and good scientific practice. The present report follows the Consolidated Standards of Reporting Trials (CONSORT) 2010 guidelines for feasibility randomised controlled trials (RCTs).52

Recruitment

Recruitment took place following an open recruitment strategy. Different methods were administered: research staff in diabetes centres and diabetes self-help groups who informed potential participants of the offer, flyers in medical practices and social media posts in diabetes-related groups. Interested people signed up on the ACTonDiabetes homepage or expressed their interest via email to the study mail address. Those who met the inclusion criteria and provided written informed consent were randomised.

Randomisation and blinding

Randomisation was performed on an individual level by a person not otherwise involved in the study (Lena Storz). The randomisation list was created by an automated web-based program called ‘sealed envelope’ (https://www.sealedenvelope.com). Lioba Fluhr enrolled the participants. A permuted block randomisation with variable 2 and 4 block size (randomly arranged) and an allocation ratio of 1:1 was used.

ACTonDiabetes intervention

The guided internet intervention was delivered on the online platform Minddistrict. The theoretical base is the ACT. Contents were adapted to the population of people with diabetes from the already evaluated ACTonPain intervention.49–51 The intervention consists of seven modules. The content of the intervention involves psychoeducation underpinned by fictional peer support (a woman with recently diagnosed type 2 diabetes, a younger man with type 1 diabetes, an older man with long-standing, insulin-treated type 2 diabetes). The narratives of the peers address typical problems and burdens, worries, needs and experiences with strategies and resources as well as topics covered in the intervention. Contents are provided by means of texts, video sequences, audio files or illustrations of various ACT models and metaphors. A description of the intervention contents can be found in table 1. Participants are advised to process through the intervention in 7 weeks, completing one module per week. The processing time for each module is scheduled to take approximately 45–60 min. ACTonDiabetes is based on three assumed effect factors: the intervention contents, guidance and daily exercises. Guidance was provided by an e-coach (psychologist) who provided standardised feedback after each module. To support transfer into everyday life, specific ACT-based exercises and tasks (eg, keeping a diabetes distress diary) were included. Furthermore, participants received short message service (SMS) coaching with motivational prompts and mindfulness tasks. A schematic depiction of the intervention can be seen in figure 1.

Figure 1

Intervention structure of ACTonDiabetes. SMS, short message service. SMART, specific, measurable, achievable, relevant, time-limited

Table 1

Overview of contents and techniques of all sessions

Measures

All surveys were conducted online via the Unipark platform (unipark.de).

Measurement time points were at baseline (T1) and at 8 weeks after randomisation (T2) (ie, after the treatment should normally be completed). An overview of outcomes, measurements and points of assessment is shown in table 2.

Table 2

Overview of constructs, measurement instruments and points of assessment

Study aims were operationalised as follows:

  1. Trial recruitment and acceptability.

    • Access routes, study flow, baseline characteristics.

    • User attitudes, formative user feedback, negative effects, adherence.

  2. Potential of the intervention to affect intended outcomes in a confirmatory trial.

    • Diabetes distress, depression, anxiety, self-management, diabetes acceptance, quality of life, fear of progression.

Trial recruitment and acceptability

Recruitment

Access routes were recorded by an open-ended question asking how participants got to know about the study. With regard to study flow, early participant attrition was investigated to determine if mechanisms sufficiently bridged the gap between eligibility/consent and actual trial uptake, as recommended.53 54 For this purpose, we measured the participation rate (number of participants divided by the number of eligible people). Recruitment was deemed successful if the participation rate was at least 70% of all eligible participants (in hoc sensu early attrition maximum 30%).54 55 In order to learn about characteristics of the population reached by applied recruitment strategies, we assessed age, gender, diabetes type and former psychotherapy/counselling experience. Additionally, we explored if participants who signed up had a certain level of burden, thus elevated symptoms of diabetes distress, depression or anxiety at baseline (T1).

Acceptability

Acceptability refers to reactions of participants regarding the ACTonDiabetes intervention.56 Collected data include attitudes towards internet interventions (Attitudes towards Psychological Online Interventions Questionnaire (APOI)57), as well as information acquired through the online platform Minddistrict on usage and engagement (number of modules completed, length of processing time per module, number of intervention completers and formative user feedback). Formative user feedback was collected to gain knowledge of the users’ acceptance of the intervention. Therefore, we assessed comments and critiques of the participants as well as the perceived appropriateness of the intervention contents. Furthermore, we assessed perceived negative effects of the intervention (Inventory for the Assessment of Negative Effects of Psychotherapy (INEP)58), as well as treatment satisfaction (Client Satisfaction Questionnaire (CSQ-8)59) using validated questionnaires.

Attitudes towards internet interventions

The APOI57 consists of 16 items (eg, ‘I think ACTonDiabetes could help me’) which are rated on a 5-point Likert scale (1=‘I do not agree at all’ to 5=‘I agree completely’). The tool estimates four subscales (four items each): scepticism and perception of risks (SCE), threat due to technology (TET), confidence in effectiveness (CON) and anonymity benefits (ABE). Higher scores on CON and ABE indicate more positive attitudes, while higher values on SCE and TET indicate more negative attitudes towards internet interventions. Subscale scores can be added to a total score (range 16–80). A higher total score indicates a more positive attitude.57 A low level of acceptance of the internet-based delivery format has been associated with a lower uptake rate.60 Thus, an at least medium level of acceptance may be required for the implementation on a larger scale.61 62 Understanding attitudes towards internet interventions may help allocating dissemination and recruitment resources for a larger RCT efficiently.62

Formative user feedback

Participants in the EG received a voluntary feedback questionnaire after each module. Questions aimed at rating the length and comprehensibility for each module on a 3-point scale (too short, just right, too long). Additional open questions were administered to gather information on certain intervention contents (exercises, techniques or metaphors) per module (‘What was the most/least helpful exercise for you within this module?’).

Negative effects

Potential negative effects were assessed using the 15-item version of the INEP.58 Participants rated possible negative effects which occurred during or after the intervention on a 4-point Likert (0=‘no agreement’ to 3=‘total agreement’) or a bipolar 7-point scale (−3=‘worse’ to 3=‘better’). Participants then indicate if they attribute negative effects to the intervention or other circumstances (eg, ‘I feel better (+3)…worse (−3) since the start of the intervention’; ‘I put this effect down to the intervention’ (1), ‘other circumstances’ (2)). Topics include possible negative effects in the fields social environment, intrapersonal factors and work-related situations.

Treatment satisfaction

The CSQ-859 measures satisfaction with the intervention using eight items and a 4-point Likert scale. Higher scores indicate higher treatment satisfaction. For psychosomatic populations, a mean of M=23.5 (SD=5.0).63 Thus, values close to M=23.5 were classified as sufficient satisfaction with the ACTonDiabetes treatment to be investigated in a larger trial.

Adherence

Study attrition as well as intervention adherence was evaluated 8 weeks after randomisation. Adherence was operationalised by the percentage of participants who completed the majority of modules. That is, participants at least processed through the introduction and the initial four of the seven core modules within 8 weeks.

Outcome data

Diabetes distress

The 20-item Problem Areas In Diabetes (PAID) Scale64 was used to measure diabetes distress. The scale requests diverse emotional problems due to living with the chronic condition. Responses are given on a 5-point Likert scale (0=‘no problem’ to 4=‘serious problem’). The raw sum score is multiplied with 1.25 to calculate the total score (range 0–100). Higher scores indicate higher diabetes distress. Values of 40 and above are considered to indicate elevated, thus clinically relevant diabetes distress.65

Depression

The Patient Health Questionnaire-9 (PHQ-966) was used to measure symptoms of depression. Its nine items assess the key symptoms of depression according to the Diagnostic and Statistical Manual of Mental Disorders; responses are given on a 4-point Likert scale (0=‘not at all’ to 3=‘almost every day’). The total score ranges from 0 to 27 with values of 10 or higher suggesting elevated depressive symptoms.

Anxiety

The Generalized Anxiety Disorder 7-item Scale (GAD-767) was used to measure symptoms of anxiety. Seven items are rated on a 4-point Likert scale (0=‘never’ to 3=‘almost every day’). Higher total scores (range 0–21) indicate higher levels of anxiety.

Self-management

Overall, diabetes self-management was measured using the Diabetes Self-Management Questionnaire (DSMQ68), consisting of 16 items which describe aspects of self-management. Items are rated on a 4-point Likert scale (0=‘does not apply to me’ to 3=‘applies to me very much’). The raw sum score is transformed to a scale from 0 to 10 with higher scores suggesting better self-management.

Acceptance

The Acceptance and Action Diabetes Questionnaire69 was used to measure diabetes acceptance. Acceptance of diabetes-related feelings, thoughts and its impact on valued action is measured on 11 items on a 5-point Likert scale (1=‘never’ to 5=‘nearly always’).

Quality of life

The Assessment of Quality of Life 8-item Questionnaire70 was used to measure quality of life on eight dimensions (independent living, senses, pain, mental health, happiness, self-worth, coping and relationships). Sum score measures indicate overall physical and psychosocial quality of life. The total scores range between 35 and 176 points with higher values indicating higher quality of life.

Fear of progression

The short form of the Fear of Progression Questionnaire71 measures worries and fear regarding disease progression and development of diabetes complications using 12 items and a 5-point Likert scale (1=‘never’ to 5=‘very often’). The total score ranges from 0 to 60, higher scores indicate higher fear.

Sample size

As this trial was intended to help revise/finalise the intervention and select suitable outcome measures for the full-scale trial, the target of this trial was to recruit at least 40 participants with 20 participants per arm. In accordance with the extended version of the CONSORT statement for feasibility trials,52 investigators decided to proceed with the recruitment of participants until enough information was reached to decide whether or how to continue with a future definitive trial. Online supplemental table 1 comprises formal feasibility criteria with regard to trial recruitment, acceptability and outcome data following standard recommendations.56 72

Data analysis

The data were analysed with R.73 Quantitative data include descriptive statistics (frequency, percentage, mean, SD, median) and linear regression models for investigating potential group differences. Regression models were used to investigate group differences (dummy coded predictor: EG=1). Baseline values were used as covariate in all regression models.74 Analyses are based on an intention-to-treat principle. Multivariate imputation by chained equations were performed to create 20 complete datasets.74 Missing data were assumed to be missing at random.75 Predictive mean matching was used as imputation method.74 Imputation models were defined following the recommendations by van Buuren et al,74 76 that is, including variables defined for the primary analysis and auxiliary variables. Analyses were conducted for each imputed dataset and pooled using Rubin’s rule.77 78 For all outcomes, mean, SD, standardised regression coefficient and the corresponding 95% CI are reported. The significance level was set to p<0.05 for all analyses.

Patient and public involvement

Patient and public involvement (PPI) representatives provide input to the present study in several stages. The intervention was further developed in a multidisciplinary team comprising psychologists, psychotherapists, diabetes specialists and people with diabetes. PPI representatives were included in the intervention development to improve content, usability and design of ACTonDiabetes.

Results

Trial recruitment and acceptability

Recruitment

The study was closed after N=42 participants had been randomised. N=61 individuals were assessed for eligibility and informed about the study. N=18 people did not consent, two participants were excluded for not meeting inclusion criteria (figure 2). Forty-two people with diabetes were randomised (participant flow, figure 2), equalling to a participation rate of 71%. Sixty-four per cent of people assessed for eligibility got to know about the study from specialised diabetes centres, 30% were recruited via social media, 6% from other sources.

Baseline participant sociodemographic and clinical characteristics are presented in table 3. Mean age of the sample was M=46.9 (SD=14.4), 50% were female. The majority, 76%, of the participants were diagnosed with type 1 diabetes.

Table 3

Baseline sample characteristics by group

Baseline diabetes distress was elevated with a mean PAID score of M=43.9 (SD=13.7). Furthermore, the mean PHQ-9 and GAD-7 scores at baseline suggested mild depressive (M=8.40, SD=5.11; PHQ-9) and anxiety symptoms (M=6.62, SD=4.34; GAD-7).

Acceptability

Attitudes towards internet interventions

The assessment of attitudes towards internet interventions using the APOI revealed values of M=39.7 (SD=7.1) at T1 and M=41.7 (SD=11.25) at T2 in the EG, and M=40.1 (SD=9.4) (T1) and M=42.6 (10.0) (T2) in the CG (see table 3). Attitudes were not significantly different between EG and CG at post-measurement (b=−0.04, p=0.86). Participants’ mean satisfaction with intervention according to the CSQ-8 total score was M=25.8 (SD=5.6) (table 3).

Formative user feedback

We received N=89 feedback forms from n=21 participants across the seven modules regarding processing time per module. Much feedback (75%, n=16) indicated that the processing time per module was just right. Minddistrict data revealed that processing through modules took on average M=84 min (SD=36) per module. Open questions revealed that mindfulness and acceptance-based interventions were perceived as particularly positive across modules (46% of 89 feedback, n=41). Across the modules, open-ended questions indicated that contents were not always easy to understand (34%, n=30), not sufficiently individualised (20%, n=18) and too text intensive in overall amount (21%, n=19).

Negative effects

At post-treatment, none of the participants of the EG indicated to feel worse than before ACTonDiabetes. About one-third of participants reported no change in their subjective well-being (33%, n=7), while two-thirds (66%, n=14) reported that their well-being improved since the start of the intervention. All participants who reported improvements attributed their experienced positive changes to the intervention. Four participants (14%) reported to suffer more from past experiences than before the intervention; one of them attributed this change to the intervention, while the others attributed it to other circumstances. One person reported a more increased number of relationship conflicts than before the intervention. However, this was not attributed to the intervention. Two participants (6.8%) reported worsened relationships with their families and three regarding friends (10.3%) since the intervention, but none of them attributed these changes to the intervention. Four persons (19%) of the EG worried that colleagues or peers might get to know about their participation in the study/receiving treatment. Three persons (10.3%) indicated to worry about possible future trouble with insurance; one of them attributed this to the intervention. Six persons (20.7%) indicated to have more financial worries than before the intervention. One of them attributed this to the intervention. Eight persons (27.5%) indicated feeling dependent on the intervention. Eleven persons (37.8%) reported greater difficulties to make decisions on their own after finishing the intervention, but only one of them attributed this to the intervention. Finally, five persons (17.2%) reported that they did not feel well for longer periods after attending the intervention but attributed this to other life circumstances.

Overall, N=16 participants of the EG (76%) reported at least one negative change in social, intrapersonal or work-related aspects. Of them, n=6 participants (38%) attributed these experienced changes to the intervention. Thus, one-third of all treated participants experienced at least one negative change due to ACTonDiabetes.

Intervention adherence

Analyses on intervention adherence revealed that nine participants of the EG (43%) completed all seven modules within 8 weeks after randomisation. Excluding participants who never started the intervention, from randomisation to post-treatment 57% (n=10) dropped out before starting module 5 (figure 3). Eleven participants provided reasons for not starting or discontinuing: three participants indicated that participation was not useful to them, eight stated that they did not have enough time for further participation. Overall, 52% of all participants finished at least module 4 after 8 weeks.

Figure 3

Intervention completion 8 weeks after randomisation.

Changes in psychometric outcomes

There was a significant difference between the groups regarding diabetes distress after the intervention (T2) favouring the EG (Cohen’s d=0.65, 95% CI −1.27 to −0.02, p=0.042). The effect adjusted for the baseline value was (b=−0.68, 95% CI −1.36 to 0.02, p=0.048, adjusted R²=0.17). Changes in the other assessed outcomes were non-significant between groups, however, all with a descriptive trend towards greater improvements in the EG (table 4).

Table 4

Linear regression analysis of changes from baseline to post-treatment

Discussion

This RCT evaluated the feasibility and potential effectiveness of an internet intervention to decrease elevated diabetes distress in people with type 1 or type 2 diabetes. To our knowledge, this is the first study that investigates an ACT-based internet intervention for this population. Participants reported elevated diabetes distress as well as depressive and anxiety symptoms, thus recruitment strategies reached people with an at least quantifiable level of psychological burden.

The participation rate in this study was at 71%, indicating that the applied procedure to transfer eligible individuals into the study is appropriate. We reached female and male participants equally; however, the majority of the participants had type 1 diabetes. This is somewhat surprising as different studies show that both groups report equal burden due to diabetes. The imbalance may be in part explained by the recruitment strategies. That is, the overall number of members in identifiable self-organised social media groups with diabetes type 1 was N=15 000, while identifiable self-organised groups for diabetes type 2 comprised only about 1000 members. Furthermore, many participants were recruited via specialised centres with an over-representation of people with type 1 diabetes compared with the primary care setting. Personal recommendation may have led to higher participation than advertisement only. Overall, the intervention seems to be particularly interesting for middle-aged persons of both sexes who treat their diabetes with insulin and are not currently undergoing psychotherapeutic treatment.

From randomisation to post-treatment, 30% of the participants dropped out, most of them discontinuing during the first half of the intervention. Only 43% of the participants finished all seven modules within 8 weeks after randomisation. However, 62% (n=13) of the participants completed the intervention within 21 weeks after randomisation, suggesting that a slower treatment performance was preferred by some people. Although the dropout is comparable with other trials in the field, offline or online33 79 future studies (including the planned full-scale trial) would benefit from adding mechanisms to foster adherence. Low intervention completion could limit the effectiveness of the intervention in a confirmatory trial. Guidance, SMS coaching and reminders might be useful techniques to keep participants involved80 81 and should be further extended. A greater variety in presentation forms, helping to clarify contents and facilitating comprehension, could be experienced as positive and help to increase participants’ adherence.82 Formative feedback on the intervention revealed that there should be less extensive and complex texts and better comprehensibility. Analyses of the processing time per module indicated that it took on average 24–39 min longer than expected to process through the intervention. However, 75% of participants indicated that the processing time was just right for them. This inconsistency might be explained by possible breaks during working on the modules. The finding of long processing times suggests that the contents should not be extended per module in the further developed version of ACTonDiabetes. Another point that was raised by the participants concerns the individualisation of contents. Higher degrees of individualisation could be realised by adding diabetes-specific aspects of living with diabetes to the case vignettes (eg, by condensing the narratives throughout the intervention). This could help to better fit the intervention contents to the target population. Additionally, more individualisation could be achieved by expanding the space for individual life stories within the intervention. This could comprise personal writing like the development of illness narratives.

More comprehensibility could be achieved by strengthening interdisciplinary exchange, that is, with regard to text comprehension researchers.83 The use of written text as a medium for conveying contents should be limited in favour of other media and interactive materials like illustrations, videos and audio files. Another yet too little investigated and integrated factor is a positive experience and a gratification character when processing through internet interventions. Interventions could be further enriched by integrating token systems or serious games (eg, games with the primary purpose of knowledge transfer).84 To optimise the ACTonDiabetes intervention based on these findings, the amount of written text should be reduced per module by replacing it with video and audio materials. Also, optimising persuasiveness of ACTonDiabetes might improve adherence.85

The attitudes towards internet interventions were generally positive. More positive attitudes may be associated with increased effectiveness of internet interventions.86 Thus, providing more detailed information about ACTonDiabetes prior to the beginning of the intervention, or the inclusion of an acceptance-facilitating intervention at the start, might evoke more positive attitudes towards the internet-based treatment, hence increasing adherence and treatment effectiveness.61 87–89

Satisfaction with the intervention was positive and comparable with results of psychological treatments in psychosomatic contexts.63 Participants reported non-severe negative effects due to the intervention. This is consistent with the current literature suggesting that negative treatment effects should be expected and thus monitored carefully.90–92 Nevertheless, almost one-third of the participants reported at least one negative change which was attributed to the intervention. This points to the importance of considering possible negative side effects of ACTonDiabetes in a larger trial. To prevent such experiences, regular assessments should be implemented.93 However, none of the participants of the EG indicated to feel worse due to the intervention. Future trials should measure both symptom deterioration and perceived negative effects during the treatment phase.93

To draw conclusions on effectiveness of the intervention regarding diabetes distress, it requires a larger study. The same holds true for potential effects on other intended outcomes like depression, anxiety and fear of progression. Likewise, effects on self-management and diabetes acceptance need to be evaluated in a larger study. Due to feasibility as primary outcome of this study, the small sample size as well as indications of inhomogeneity between the groups regarding prior psychotherapy/counselling experiences and educational level, conclusions on effectiveness are not subject to this study.

Limitations of this study comprise the fact that all data are based on self-report. Future studies should at least rely on professional-assured diagnosis. Furthermore, the absence of HbA1c data is one of the main shortcomings of this study. Future studies should incorporate medical data like HbA1c values as the evaluation of potential changes in HbA1c might play a key role regarding the relevance of the intervention in diabetes care. Additionally, comorbid disorders could be assessed in future studies to achieve better insights into the physical conditions of participants.

Another limitation is that the study tested the EG against a waitlist CG with participants being a priori informed about the difference between the groups. Additionally, participants in the EG received the guided version of ACTonDiabetes while the CG received the unguided ACTonDiabetes intervention. Thus, effects of waiting for treatment and receiving ACTonDiabetes without guidance could have biased the data. For psychotherapy research in general, small effect sizes found in waitlist control groups suggest that testing a treatment against a waitlist might not be a very strict test.94 Future trials should use enhanced treatment-as-usual groups or an attention placebo control group to avoid these limitations.

Finally, the current sample was not recruited in a naturalistic setting, thus it may not reflect the real-life uptake of patients in the healthcare system. In order to investigate this, a pragmatic trial would have to be conducted which systematically recruits participants from routine care setting. In addition to this, no exact data were obtained on the number of people who were invited to participate. A future trial should address this shortcoming to allow the evaluation of the proportion of individuals reached from the potential eligible population.

Although generalisability of results is arguably limited, an important strength of this trial is the provision of deeper insights into evidence on internet-based mental health support for people with diabetes. A major strength is that we tested whether the intervention is feasible prior to implementing it on a larger scale. The intervention will be further optimised on the basis of the present findings prior to proceeding to the definitive trial.

A confirmatory trial will be needed to support the present preliminary findings and draw firm conclusions about treatment effects of ACTonDiabetes.

This paper may be fruitful for researchers planning studies or developing internet interventions for people with diabetes or other chronic conditions and comorbid psychological burden. ACT-based interventions constitute a promising approach in this context. New interventions for diabetes distress in people with type 1 or type 2 diabetes are needed. ACT could be particularly effective for people with diabetes as it focuses on the acceptance of unchangeable circumstances more specifically than standard CBT. The present results support that ACT-based interventions may be beneficial for people with diabetes. Strategies to foster adherence as well as content modifications according to the present results will be implemented to address key barriers to continued use and increase treatment effectiveness regarding diabetes distress.

ACTonDiabetes will be investigated in a subsequent full-scale trial. Trial registration number: DRKS00016738.

Data availability statement

Data are available upon reasonable request.

Ethics statements

Ethics approval

All procedures involved in the study are consistent with the generally accepted standards of ethical practice as approved by the ethics committee of the University of Ulm (file number 283/17).

Acknowledgments

We kindly thank Yannik Terhorst for verification of imputation procedures and statistics. We kindly thank Lena Storz for running the randomisation procedure. We kindly thank Agnes Geirhos and Pauline Meyer for e-coaching the participants. We kindly thank Lioba Fluhr for e-coaching participants and helping with the operative performance of the study. We kindly thank the people living with diabetes who gave their feedback in the development phase of the intervention.

References

Supplementary materials

  • Supplementary Data

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Footnotes

  • Twitter @EileenBendig

  • Contributors EB, NB and HB designed and planned the study. ACTonDiabetes builds on ACTonPain (Jiaxi Lin) and was developed by the Department of Clinical Psychology and Psychotherapy at Ulm University (lead developer EB). The supervision was realised in a hierarchical structure with HB supervising EB who supervised project staff throughout the study. EB operatively performed the study. EB analysed and interpreted the data. EB drafted the manuscript. PA and AS critically revised the manuscript. AS additionally audited the manuscript for important intellectual content. All authors approved the final version to be published and agree to be accountable for all aspects of the work.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests HB has received fees for lectures/workshops and consultancy fees from chambers of psychotherapists, psychological and medical associations and training institutes for psychotherapists as well as several third party-funded grants in the e-mental health context. All other authors report no conflicts of interest regarding this work.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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