Article Text

Interventions to increase immunisation coverage among children 12–23 months of age in India through participatory learning and community engagement: pilot study for a cluster randomised trial
  1. Mira Johri1,2,
  2. Dinesh Chandra3,
  3. Georges K Koné1,
  4. Sakshi Dudeja3,
  5. Marie-Pierre Sylvestre1,4,
  6. Jitendar K Sharma5,
  7. Smriti Pahwa3
  1. 1Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, Québec, Canada
  2. 2Département d'administration de la santé, École de santé publique, Université de Montréal, Montréal, Québec, Canada
  3. 3Pratham Education Foundation (ASER Centre), New Delhi, India
  4. 4Département de medicine sociale et preventive, École de santé publique, Université de Montréal, Montréal, Québec, Canada
  5. 5National Health Systems Resource Centre (NHSRC), Ministry of Health and Family Welfare, Government of India, New Delhi, India
  1. Correspondence to Dr Marie-Pierre Sylvestre; marie-pierre.sylvestre{at}umontreal.ca

Abstract

Objective With the aim of conducting a future cluster randomised trial to assess intervention impact on child vaccination coverage, we designed a pilot study to assess feasibility and aid in refining methods for the larger study.

Trial design Cluster-randomised design with a 1:1 allocation ratio.

Methods Clusters were 12 villages in rural Uttar Pradesh. All women residing in a selected village who were mothers of a child 0–23 months of age were eligible; participants were chosen at random. Over 4 months, intervention group (IG) villages received: (1) home visits by volunteers; (2) community mobilisation events to promote immunisation. Control group (CG) villages received community mobilisation to promote nutrition. A toll-free number for immunisation was offered to all IG and CG village residents. Primary outcomes were ex-ante criteria for feasibility of the main study related to processes for recruitment and randomisation (50% of villages would agree to participate and accept randomisation; 30 women could be recruited in 70% of villages), and retention of participants (50% of women retained from baseline to endline). Clusters were assigned to IG or CG using a computer-generated randomisation schedule. Neither participants nor those delivering interventions were blinded, but those assessing outcomes were blinded to group assignment.

Results All villages contacted agreed to participate and accepted randomisation. 36 women were recruited per village; 432 participants were randomised (IG n=216; CG n=216). No clusters were lost to follow-up. The main analysis included 86% (373/432) of participants, 90% (195/216) from the IG and 82% (178/216) from the CG.

Conclusions Criteria related to feasibility were satisfied, giving us confidence that we can successfully conduct a larger cluster randomised trial. Methodological lessons will inform design of the main study.

Trial registration number ISRCTN16703097

  • INFECTIOUS DISEASES
  • PUBLIC HEALTH

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