Impact Evaluation of Türkiye's Adolescent Girls' and Boys' Empowerment Programme for Elimination of Child Marriage

April 18, 2025 updated by: Yasemin Kisbu, UNICEF
Low income, refugee, displaced and disaster affected populations face a variety of protection risks, including higher risk of child, early and forced marriage and unions (CEFMU). This is the case in Türkiye, where low income, refugee populations and those affected by the 2023 earthquake in Southern and Central Türkiye face elevated risk of child marriage. As part of the UNICEF Türkiye Country Office (TCO) commitment to implement comprehensive interventions that aim to contribute to a change in social norms and attitudes towards gender equality, the CO and partners have developed the "Adolescent Girls' and Boys' Empowerment for Elimination of Child Marriage" program (hereafter "the program"). The program is an 8-week group-based empowerment and life skills training for adolescent girls aged 12 - 18 years old, a 4-session adolescent boys awareness training, and a one-time awareness raising seminar for caregivers. The current trial has the overall objective of evaluating the short-term causal impact of the program with respect to CEFMU and related outcomes for adolescent girls. The trial design is an individual randomized control trial, allocating 820 households with adolescent girls to either treatment or control on a 1:1 basis. The primary data collection includes a pre- and post-intervention caregiver and adolescent face-to-face survey, as well as a one-time qualitative data collection. The trial results will inform the future operation and scale-up of the program, as well as contribute to the broader evidence base on what works to increase the empowerment of adolescent girls and reduce CEFMU.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Low income, refugee, displaced and disaster affected populations face a variety of protection risks, including higher risk of child, early and forced marriage and unions (CEFMU). This is the case in Türkiye, where low income, refugee populations and those affected by the 2023 earthquake in Southern and Central Türkiye face elevated risk of child marriage. As part of the UNICEF Türkiye Country Office (TCO) commitment to implement comprehensive interventions that aim to contribute to a change in social norms and attitudes towards gender equality, the CO and partners have developed the "Adolescent Girls' and Boys' Empowerment for Elimination of Child Marriage" program (hereafter "the program"). The program is an 8-week group-based empowerment and life skills training for adolescent girls aged 12 - 18 years old, a 4-session adolescent boys awareness training and a one-time awareness raising seminar for caregivers. The current trial has the overall objective of evaluating the short-term causal impact of the program with respect to CEFMU and related outcomes for adolescent girls. The trial seeks to answer the following evaluation questions:

  • 1) Does the program improve participant adolescent girls' agency, self-confidence, and gender-equitable attitudes (including for CEFMU), and to what extent?
  • 2) Does the program improve the household enabling environment, including gender-equitable attitudes (including CEFMU), social support, protective behaviors against CEFMU, and use of social services among participating caregivers and in the broader community, and to what extent?
  • 3) Does the program reduce CEFMU for adolescent girls, and to what extent?
  • 4) Through which pathways (or combination of pathways) do potential impacts occur?
  • 5) Was the program implemented in a manner to maximize potential impacts? and
  • 6) What is the return-on-investment (cost-benefit calculation) for the program? The trial design is an individual randomized control trial, allocating 820 households with adolescent girls to either treatment or control on a 1:1 basis. The primary data collection includes a pre- and post-intervention caregiver and adolescent face-to-face survey, as well as a one-time qualitative data collection. The trial results will inform the future operation and scale-up of the program, as well as contribute to the broader evidence base on what works to increase the empowerment of adolescent girls and reduce CEFMU.

Study Type

Interventional

Enrollment (Estimated)

820

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Yasemin Kisbu, Ph.D.
  • Phone Number: +90 532 215 37 90
  • Email: ykisbu@unicef.org

Study Contact Backup

Study Locations

      • Ankara, Turkey
        • UNICEF Türkiye
        • Contact:
        • Contact:
        • Contact:
          • Tuna Kılınç, M.Sc.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion criteria (primary study participant, however note that primary female caregivers and siblings will be invited to participate in the study pending inclusion of primary study participant):

  • Adolescent girls aged 12 - 17 years
  • Unmarried girls
  • Have never previously been exposed to the intervention
  • Live in a family or household with at least one adult caregiver
  • Live in a family who are social service clients of the implementing partner
  • Live in a family who are risk-assessed as 'low' or 'medium' on the family risk assessment tool
  • Live in a family which is planning on staying in the catchment area of the intervention in the subsequent 6-months

Exclusion criteria:

  • Adolescent girls younger than 12 or older than 17 years
  • Girls who are married or cohabiting
  • Previously been exposed to the intervention
  • Are in institutionalized or non-family-based care
  • Live in a family who are not social service clients of the implementing partner
  • Live in a family who are risk-assessed as 'high' or 'highest' on the family risk assessment tool
  • Live in a family which is planning on moving outside the catchment area of the intervention in the subsequent 6-months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Adolescent Girls' and Boys' Empowerment Program
Adolescent Girls' and Boys' Empowerment Program for Elimination of Child Marriage

The program was developed based on a social behavioural change (SBC) approach in order to change attitudes and behaviours of the participants, consisting of the following main activities on a 6 - 8 week cycle.

  • Girls' Empowerment Training: Workshops comprise six sessions of approximately 80 minutes each, held separately with girls aged 12-15 and 16-18 years in groups of approximately 12-20 adolescents on a range of life skill themes.
  • Boys' Awareness Raising Training: Similar to the girls' training, four workshops are organized for boys aged 12-15 and 16-18 years, in separate sessions, with similar length and group size.
  • Awareness Raising Seminars to Caregivers: Caregivers (e.g., mothers, fathers) are invited to a one-time seminar focused on the negative outcomes of child marriage and role of caregivers in preventing child marriage, lasting approximately one hour and conducted separately for fathers and mothers to eventually influence social norms in the family and communities.
No Intervention: Control
Business as usual (delayed intervention, post-trial - if funding allows)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of girls married or cohabiting
Time Frame: Baseline and 8-weeks post-intervention
Marriage or cohabitation status measured among adolescent girls
Baseline and 8-weeks post-intervention
Score on new general self-efficacy scale (short form, higher is better)
Time Frame: Baseline and 8-weeks post-intervention
Eight-item scale asking about internal efficacy, with response options on a five-point scale, ranging from 1 = strongly disagree, to 5 = strongly agree (score ranges from 8 - 40). Widely used scale for individual ability to achieve goals across a range of different situations, despite difficulties. Interpreted as a sub-component of the construct of adolescent girls' agency.
Baseline and 8-weeks post-intervention
Score on decision-making scale (higher is better)
Time Frame: Baseline and 8-weeks post-intervention
Ten-item scale asking about freedom to make choices across domains, with response options on a four-point scale, ranging from 1 = not at all, to 4 = a large extent (score ranges from 10 - 40). Adapted from the program version of the women's empowerment in agriculture index (pro-WEAI) to include adolescent-specific questions, previously piloted in Ethiopia among male and female youth. Interpreted as a sub-component of the construct of adolescent girls' agency.
Baseline and 8-weeks post-intervention
Score on voice scale (higher is better)
Time Frame: Baseline and 8-weeks post-intervention
Eight-item scale asking about girls' ability to share feelings and speak up in different scenarios, with response options on a four-point scale, ranging from 1 = never, to 4 = all of the time (score ranges from 8 - 32). Voice scale is adapted from Global Early Adolescent Survey and interpreted as a sub-component of the construct of adolescent girls' agency.
Baseline and 8-weeks post-intervention
Score on child marriage attitudes scale (higher is better)
Time Frame: Baseline and 8-weeks post-intervention
Thirteen-item scale developed and piloted in Türkiye by the author team to measure child marriage attitudes, with response options on a four-point scale, ranging from 1 = strongly disagree to 4 = strongly agree. The scale is measured among adolescent girls and boys, as well as their caregivers (score ranges from 13 - 52).
Baseline and 8-weeks post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Scale of perceived social support (higher is better).
Time Frame: Baseline and 8-weeks post-intervention
The family and friends' sub-scales of the multi-dimensional scale of perceived social support (MSPSS) consisting of nine questions answered on a four-point scale, ranging from 1 = strongly disagree to 4 = strongly agree. The scale is measured among adolescent girls and ranges from 9 - 36.
Baseline and 8-weeks post-intervention
The Balanced Cohesion subscale of the Family Adaptability and Cohesion Evaluation Scale (higher is better)
Time Frame: Baseline and 8-weeks post-intervention
The Balanced Cohesion subscale of the Family Adaptability and Cohesion Evaluation Scale is a seven-item scale answered on a five-point scale, ranging from 1 = strongly disagree to 5 = strongly agree. The scale is measured among caregivers and ranges from 7 - 35.
Baseline and 8-weeks post-intervention
The Revised Family Communication Pattern Instrument Conversation Orientation Sub-scale (higher is better)
Time Frame: Baseline and 8-weeks post-intervention
The Revised Family Communication Pattern Instrument Conversation Orientation Sub-scale measures parent-adolescent communication and is a 15-item scale answered on a five-point scale, ranging from 1 = strongly disagree to 5 = strongly agree. The scale is administered to caregivers and ranges from 15 - 75.
Baseline and 8-weeks post-intervention
Score on willingness to intervene and speak out for girls' scale (higher is better)
Time Frame: Baseline and 8-weeks post-intervention
Willingness to speak out and take action to support girls measured using simple self-reported questions on willingness to speak up against harmful behaviors: 1) child marriage, 2) violence against girls, 3) girls' rights and 4) for girls in times of need. These four domains are each assessed using one question answered on a four-point scale, ranging from 1 = strongly disagree to 4 = strongly agree. The scale is measured among adolescent boys and caregivers and ranges from 4 - 32.
Baseline and 8-weeks post-intervention
Linkages to services scale (higher is better)
Time Frame: 8-weeks post-intervention
Received assistance or benefits from services measured among adolescent girls and caregivers, collected as a simple sum = 1 if received any services from: 1) health, 2) social, or 3) legal services (ranges from 0 - 3)
8-weeks post-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Zlata Bruckauf, Ph.D., UNICEF

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 21, 2025

Primary Completion (Estimated)

October 30, 2025

Study Completion (Estimated)

October 30, 2025

Study Registration Dates

First Submitted

April 7, 2025

First Submitted That Met QC Criteria

April 18, 2025

First Posted (Actual)

April 27, 2025

Study Record Updates

Last Update Posted (Actual)

April 27, 2025

Last Update Submitted That Met QC Criteria

April 18, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • HML2855

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Data from the trial will be owned by UNICEF and efforts will be made to share the deindentified data in a public repository, pending UNICEF approval. In addition, it is expected that de-identified replication files will be made publicly available upon the publication of any journal articles to allow the reproduction of all tables, figures and results, alongside statistical replication code.

IPD Sharing Time Frame

IPD will be available 24 months after the trial ends, or upon publication of the main trial results, with no end date projected.

IPD Sharing Access Criteria

It is expected that data will be accessible to all the scientific community via open repository.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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