Narrative Therapy for Anxiety and Depression in Palestinian Refugee Adolescents
NT-AD
Effectiveness of Narrative Therapy in Reducing Anxiety and Depression Among Middle School Students in Refugee Camps in Northern Palestine: A Quasi-Experimental Study
2 other identifiers
interventional
120
1 country
1
Brief Summary
This study evaluated whether a culturally adapted 10-week narrative therapy program could reduce anxiety and depression symptoms among middle school students living in refugee camps in Northern Palestine. Adolescents aged 12-15 years from UNRWA-operated schools with moderate-to-severe anxiety and depression symptoms participated. The study used a quasi-experimental design with 120 students assigned to either the narrative therapy program (n=60) or standard school services (n=60). The 10-week program included weekly 60-minute group sessions that incorporated Palestinian cultural metaphors such as sumud (steadfastness) and olive tree symbolism. Participants completed the Revised Children's Anxiety and Depression Scale (RCADS) at three time points: before the program, immediately after the 10-week intervention, and three months later. The study measured changes in anxiety and depression symptoms, clinical improvement, and feasibility outcomes including retention, fidelity, and acceptability. Results showed that participants in the narrative therapy program experienced greater reductions in anxiety and depression symptoms compared to those receiving standard school services. The effects were maintained at the three-month follow-up. Seventy-two percent of intervention participants achieved clinically significant improvement compared to 21% of controls. The program demonstrated high retention (95%), good implementation fidelity (87.3%), and strong acceptability (85% of participants found the cultural metaphors helpful). The findings suggest that culturally adapted school-based narrative therapy may be a feasible and promising approach for addressing mental health needs among refugee adolescents in humanitarian settings. However, because this was not a randomized controlled trial, the results should be interpreted as associations rather than definitive causal effects.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable anxiety
Started Jun 2024
Shorter than P25 for not_applicable anxiety
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 16, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 14, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 14, 2024
CompletedFirst Submitted
Initial submission to the registry
June 30, 2026
CompletedFirst Posted
Study publicly available on registry
July 8, 2026
CompletedJuly 8, 2026
July 1, 2026
3 months
June 30, 2026
July 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Anxiety and Depression Symptoms
Change in total score on the Revised Children's Anxiety and Depression Scale (RCADS) from baseline to post-intervention and from baseline to 3-month follow-up. The RCADS is a 47-item self-report questionnaire measuring anxiety and depression symptoms across six subscales: separation anxiety (7 items), social phobia (9 items), generalized anxiety (6 items), panic disorder (9 items), obsessive-compulsive disorder (6 items), and major depression (10 items). Items are rated on a 4-point scale (0 = never, 1 = sometimes, 2 = often, 3 = always), with higher scores indicating greater symptom severity.
Baseline (pre-intervention), immediately post-intervention (Week 10), and 3-month follow-up
Study Arms (2)
Arm 1 (Intervention) Narrative Therapy Program
EXPERIMENTALParticipants received a 10-week culturally adapted narrative therapy program delivered in weekly 60-minute group sessions. The program incorporated Palestinian cultural metaphors including sumud (steadfastness) and olive tree symbolism, and focused on problem externalization, agency restoration, and collective resilience.
Arm 2 (Control) Standard School Services
NO INTERVENTIONParticipants received standard school-based services including regular educational activities, social skills activities, music/art therapy, and sports activities as typically provided in UNRWA-operated schools. Individual counseling was available but limited.
Interventions
A 10-week manualized narrative therapy program delivered in weekly 60-minute group sessions. The program integrates Palestinian cultural metaphors including sumud (steadfastness) and olive tree symbolism. Key components include problem externalization (using shadow and cloud metaphors), agency restoration (identifying personal strengths and resilience stories), collective resilience (community narratives), mindfulness practices, and future-oriented narrative reconstruction. Each session follows a structured format including check-in, main activity, discussion, and closing reflection. The program was delivered by trained school counselors and psychologists in UNRWA-operated middle schools.
Eligibility Criteria
You may qualify if:
- Middle school students in grades 6-9
- Aged 12-15 years
- Moderate-to-severe symptoms of anxiety and depression as measured by the Revised Children's Anxiety and Depression Scale (RCADS T-scores ≥ 65)
- Written informed consent from parent or legal guardian
- Written assent from the student
- Enrolled in a UNRWA-operated middle school in one of the participating refugee camps (Jenin, Balata, or Askar)
You may not qualify if:
- Current involvement in other mental health interventions or psychotherapy
- Severe psychiatric disorders requiring specialist care (e.g., psychosis, bipolar disorder, severe eating disorders)
- Inability to complete study assessments due to language or cognitive barriers
- Severe emotional or behavioral difficulties that would prevent participation in group sessions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Nablus University for Vocational and Technical Education, Ibn Sina College for Health Professions
Nablus, West Bank, P401, Palestinian Territories
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Masking Details
- Complete blinding was not feasible due to the nature of the behavioral intervention.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Prof in Mental Health Nursing
Study Record Dates
First Submitted
June 30, 2026
First Posted
July 8, 2026
Study Start
June 16, 2024
Primary Completion
September 14, 2024
Study Completion
December 14, 2024
Last Updated
July 8, 2026
Record last verified: 2026-07