Assessing the Feasibility and Acceptability of Watching Queen of Katwe as a Role Model Intervention Among Adolescents in High Schools in Kenya

July 17, 2025 updated by: Shamiri Institute

This study will test whether using the film Queen of Katwe as a role model story can help motivate and engage high school students in Kenya. The film is based on the true story of Phiona Mutesi, a Ugandan girl who becomes a chess champion despite growing up in poverty. The study will take place in a mixed secondary school in Ngong town, Kajiado County, with about 250 students aged 13 to 19. Students will watch the film at school. To see if the approach works well, researchers will collect data before and after the film showing.

They will check:

  1. Feasibility (how easy it is to carry out, including costs and logistics)
  2. Acceptability (how students and teachers feel about it)
  3. Engagement (how involved students are) Surveys and focus groups will be used to gather feedback. The goal is to see if this low-cost method could be used more widely to support learning and motivation in schools.

Study Overview

Status

Recruiting

Conditions

Detailed Description

This study examines the feasibility and acceptability of using the film Queen of Katwe-which tells the true story of Phiona Mutesi, a Ugandan girl from an underprivileged background who becomes a chess champion-as a role model intervention to inspire motivation and academic engagement among adolescents in high school students in Kenya. Media-based interventions have gained recognition as effective tools for promoting student learning and well-being, yet their implementation in school settings remains underexplored. This study will employ a feasibility study design and be conducted in a mixed secondary school in Ngong town, Kajiado County, Kenya, with a sample of ~250 students aged 13-19 years. Students will watch Queen of Katwe in their school setting, and data will be collected before and after the intervention to assess feasibility, acceptability, and engagement. Feasibility will be evaluated based on logistical observations, cost analysis, and the Feasibility of Intervention Measure. Acceptability will be assessed through a screening survey using the Acceptability of Intervention Measure, while focus group discussions with students and teachers will provide qualitative insights. The findings will offer valuable evidence on the potential of media-based interventions to enhance motivation and academic engagement in Kenyan schools. If found feasible and acceptable, this low-cost, scalable approach could inform future educational policies and programs aimed at supporting student aspirations and learning outcomes.

Study Type

Interventional

Enrollment (Estimated)

250

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

Study Locations

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
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Participants must be high school students in the selected school.
  • Participants must be between the ages of 13 to 19.

Exclusion Criteria:

  • There will be no other exclusion criteria.

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Shamiri Queen of Katwe
The session itself will take approximately two hours-this includes student assembly, an introduction to the study, and the screening of Queen of Katwe
The intervention involves screening the film Queen of Katwe to high school students in a school setting.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean change in aspiration score from baseline on the Aspirations Index through study completion
Time Frame: From baseline through endline, an average of two days
Changes in self-reported aspirations as measured by the Aspiration Index is used to assess long term aspirations and goals that individuals hope to accomplish in their lives. In this study, we will use a shortened 15-item version of this scale including items on aspirations of wealth, fame, image, personal growth, relationship, community and health. The scores for each item ranges between 1-7, with higher scores indicating higher aspirations.
From baseline through endline, an average of two days
Mean change in school engagement score from baseline on the School Engagement Measure through study completion.
Time Frame: From baseline through endline, an average of two days
Changes in self-reported school engagement as measured by the School Engagement Measure refer to a student's emotional, behavioural, and cognitive involvement in school activities and learning. This is a 19-item measure with responses measured on a 5-point Likert scale ranging from 1 (not at all true) to 5 (very true). Higher scores indicate greater school engagement.
From baseline through endline, an average of two days
Change in academic performance as measured using the average grades
Time Frame: Periprocedural - From academic exam results pre-intervention to academic exam results post-intervention, up to three months
Changes in academic performance as measured using the average grades obtained from the most recent exam prior to the intervention, and the first available exam following the implementation of the intervention.
Periprocedural - From academic exam results pre-intervention to academic exam results post-intervention, up to three months
Mean score of the Feasibility of Intervention Measure at study completion
Time Frame: At study completion, up to three months
Feasibility of Intervention Measure tracks metrics such as ease of setting up the screenings, logistical challenges, and time constraints. It assesses the extent to which an intervention can be successfully implemented within a given setting. This is a 4-item measure with responses measured on a 4-point Likert scale ranging from 1 (Completely disagree) to 5 (Completely agree). Higher scores indicate a better outcome, good scores on the feasibility of the intervention.
At study completion, up to three months
Mean score of the Acceptability of Intervention Measure at study completion
Time Frame: At study completion, up to three months
Acceptability of Intervention Measure assess the acceptability of the intervention by participants. This 4-item measure evaluates stakeholders' perception of an intervention's acceptability, determining whether they find it agreeable, satisfactory, or palatable. Responses are measured on a 4-point Likert scale ranging from 1 (Completely disagree) to 5 (Completely agree). Higher scores indicate a better outcome, the acceptability of the intervention.
At study completion, up to three months
Mean score of the Intervention Appropriateness Measure at study completion
Time Frame: At study completion, up to three months
Intervention Appropriateness Measure assesses perceptions of participants' intervention appropriateness. It measures the perceived fit, relevance, or compatibility of an intervention within a particular context. This 4-item measure determines whether an intervention aligns with the needs of a specific population, organisational goals, or existing workflows. Responses are measured on a 4-point Likert scale ranging from 1 (Completely disagree) to 5 (Completely agree). Higher scores indicate a better outcome, the appropriateness of the intervention.
At study completion, up to three months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Tom L Osborn, Shamiri Institute

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 (Actual)

July 3, 2025

Primary Completion (Estimated)

July 23, 2025

Study Completion (Estimated)

August 30, 2025

Study Registration Dates

First Submitted

June 30, 2025

First Submitted That Met QC Criteria

July 17, 2025

First Posted (Estimated)

July 18, 2025

Study Record Updates

Last Update Posted (Estimated)

July 18, 2025

Last Update Submitted That Met QC Criteria

July 17, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The investigators intend to share fully de-identified data through publications and upon request.

IPD Sharing Time Frame

Beginning 3 months and ending 3 years following article publication.

IPD Sharing Access Criteria

Access to study reports and protocols will be open. Access to de-identified individual participant data will be available upon request from the study team.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • 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

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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