- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07072741
- Original Trial
Assessing the Feasibility and Acceptability of Watching Queen of Katwe as a Role Model Intervention Among Adolescents in High Schools in Kenya
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:
- Feasibility (how easy it is to carry out, including costs and logistics)
- Acceptability (how students and teachers feel about it)
- 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
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tom L Osborn
- Phone Number: +254 706 408 811
- Email: osborn@shamiri.institute
Study Locations
-
-
-
Nairobi, Kenya, 00300
- Not yet recruiting
- Shamiri Institute
-
Contact:
- Rosine Baseke
- Phone Number: +254797326413
- Email: baseke@shamiri.institute
-
Contact:
- Ray Kongong'a
- Phone Number: +254797326413
- Email: ray.kongong'a@shamiri.institute
-
Nairobi, Kenya
- Recruiting
- Shamiri Institute
-
Contact:
- Rosine Baseke
- Phone Number: +254797326413
- Email: baseke@shamiri.institute
-
Contact:
- Ray Kongong'a
- Phone Number: +254797326413
- Email: ray.kongong'a@shamiri.institute
-
Principal Investigator:
- Tom Osborn
-
Sub-Investigator:
- Rosine Baseke
-
Sub-Investigator:
- Ray Kongong'a
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Tom L Osborn, Shamiri Institute
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Shamiri Queen of Katwe Project
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
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
Studies a U.S. FDA-regulated device product
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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