- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01001286
Questscope Non-Formal Education Impact Study (QSNFEIS)
This randomized controlled trial (RCT) evaluates the effectiveness of Questscope Non-Formal Education (QS NFE) on impacting psychosocial outcomes for out-of-school youth, ages 13-21, in Jordan. QS NFE is an empowerment-based education program. A unique agreement with the Jordanian Ministry of Education enables participating youth to receive a 10th-grade equivalent certificate upon successful completion of the 24-month non-formal education. The main components of QS NFE include retraining formal education teachers for fostering positive relationships with at-risk youth, asset-building learning and social activities, and a youth-driven learning environment.
The study hypothesis is that by engaging youth in positive relationships with local teachers and enabling the youth to drive the learning experience, the intervention will have positive impacts on general self-efficacy, social supports, social skills, and strengths and difficulties.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized controlled trial (RCT) evaluates the effectiveness of Questscope Non-Formal Education (QS NFE) on impacting psychosocial outcomes for out-of-school youth, ages 13-21, in Jordan. QS NFE is an empowerment-based education program. A unique agreement with the Jordanian Ministry of Education enables participating youth to receive a 10th-grade equivalent certificate upon successful completion of the 24-month non-formal education. The main components of QS NFE include retraining formal education teachers for fostering positive relationships with at-risk youth, asset-building learning and social activities, and a youth-driven learning environment.
The study hypothesis is that by engaging youth in positive relationships with local teachers and enabling the youth to drive the learning experience, the intervention will have positive impacts on general self-efficacy, social supports, social skills, and strengths and difficulties.
Youth will be recruited according to normal Questscope recruitment procedures by program leaders in five poverty pocket communities in Amman, Jordan. Six QS NFE centers will be involved in the impact evaluation (four male centers and 2 female centers). Youth will be recruited, enrolled, and randomized on an individual basis until each NFE center's sample target is met (between 24 and 40 youth, depending on the center). The overall sample target is 200 for the six NFE centers aggregately (100 intervention group and 100 waitlist comparison). The study aims to recruit 54 females and 146 males.
Randomization will be conducted electronically using a random permuted block method through SealedEnvelope.com. Data collection for outcome measures will involve a computer-based, self-administered questionnaire designed with The Survey System software by Creative Research Systems. The computer-based survey will provide both text and audio to accommodate low literacy levels.
In the event that a participant rejects his/her random assignment within 48 hours of enrollment, the youth will be replaced in the study and will not be included in final data analysis. Additionally, all siblings recruited together into the study will be blocked and randomized together in enrollment.
Study Type
Enrollment (Anticipated)
Phase
- Phase 2
Contacts and Locations
Study Locations
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-
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Amman, Jordan
- Al Mutasm School
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Amman, Jordan
- Al Urdan School
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Amman, Jordan
- Al Zubaidieh School
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Amman, Jordan
- Ali Reda Al Rekabi School
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Amman, Jordan
- Mauth Bin Jabal School
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Amman, Jordan
- Umama Bint Abi Al A'as
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age 13-18 males or 13-21 females
- out of the formal education system for more than six months
Exclusion Criteria:
- has already participated in QS NFE
- not in the above-specified age range
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Youth Club
The intervention will be compared to a waitlist comparison group.
The group will enter NFE after the four-month posttest.
During the four months, the youth will be offered a biweekly recreational youth club.
The club will be led by Jordanian university student volunteers out of community-based organizations.
Club activities will take place approximately every two weeks, including games, sports, arts and crafts, cultural activities, and trips.
The Club will not include any significant education components or youth empowerment methodology--the hypothesized active ingredients of QS NFE.
|
Participation in two-hour classes for three to five days per week. Duration involves 24 months of programming (three, eight-month learning cycles), but this randomized controlled trial will only assess impacts of participation in the first four months. Regular presence of trained, supportive adults. Educational topics and class activities determined by the youth as a group with the support of the adult teachers ("facilitators"). |
|
Experimental: Questscope Non-Formal Education
Participation in two-hour classes for three to five days per week. Duration involves 24 months of programming (three, eight-month learning cycles), but this randomized controlled trial will only assess impacts of participation in the first four months. Regular presence of trained, supportive adults. Educational topics and class activities determined by the youth as a group with the support of the adult teachers ("facilitators"). |
Participation in two-hour classes for three to five days per week. Duration involves 24 months of programming (three, eight-month learning cycles), but this randomized controlled trial will only assess impacts of participation in the first four months. Regular presence of trained, supportive adults. Educational topics and class activities determined by the youth as a group with the support of the adult teachers ("facilitators"). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
self-reported general self-efficacy
Time Frame: pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
|
self-reported social skills
Time Frame: pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
|
self-reported strengths and difficulties
Time Frame: pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
|
self-reported social supports
Time Frame: pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
pretest at enrollment (October 2009-January 2010) and 4 months following pretest
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- QS-001
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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