Implementation Science and Impact Evaluation of PfR Programme: A Hybrid cRCT Design

NCT05105373 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3162

Last updated 2023-12-04

No results posted yet for this study

Summary

The Implementation science and impact evaluation of PfR programme: A hybrid cRCT design study will use an effectiveness-implementation hybrid type 2 design to a) determine the effectiveness and cost-effectiveness of PfR, and b) determine the feasibility and impact of three different implementation strategies in terms of programme delivery. A cluster randomised controlled trial (cRCT) will examine the effectiveness, cost-effectiveness, and implementation of the Parenting for Respectability (PfR) programme on the reduction of violence against children and gender based violence in comparison to those receiving an hour lecture on parenting in the Wakiso and Amuru districts of Uganda (N = 54 clusters, 2,160 parents, 1,080 children, 1:1 allocation ratio).

Conditions

  • Parenting
  • Gender-based Violence
  • Child Maltreatment
  • IPV

Interventions

BEHAVIORAL

Parenting for Respectability

The programme addresses main challenges of Parenting and builds skills in 4 main areas 1. Poor parental bonding and child attachment; 2. Harsh parenting 3. Inequitable socialisation by gender 4. Parental conflict.

Sponsors & Collaborators

  • University of Glasgow

    collaborator OTHER
  • Oak Foundation

    collaborator OTHER
  • Network of European Foundations

    collaborator UNKNOWN
  • University of Oxford

    collaborator OTHER
  • Makerere University

    lead OTHER

Principal Investigators

  • Dr. Godfrey Siu, PHD · Child Health and Development Centre, Makerere University

  • Dr. Jamie M. Lachman, D.PHIL · University of Glasgow: MRC/CSO Social and Public Health Sciences Unit

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-06
Primary Completion
2022-08-31
Completion
2022-12-30

Countries

  • Uganda

Study Locations

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Read the full study record

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View NCT05105373 on ClinicalTrials.gov