CA-CBTCulturally Adapted CBT for Depression in Arab and Asian Adolescents in UAE
Culturally Adapted Cognitive Behavioural Therapy (CA-CBT)
+ Treatment-as-Usual (TAU)
Psychological Well-Being+5
+ Anxiety Disorders
+ Behavior
Treatment Study
Summary
Study start date: June 15, 2024
Actual date on which the first participant was enrolled.This study explores the effectiveness of a specially adapted form of therapy called Culturally Adapted Cognitive Behavioral Therapy (CA-CBT) for treating depression among adolescents in the United Arab Emirates. It focuses on teenagers aged 13-18 from Arab, Filipino, and other Asian backgrounds who show signs of depression. The therapy is designed to consider cultural factors like family stress and spiritual concerns, aiming to improve mental health care by making it more relevant to the participants' cultural contexts. The goal is to see if this approach can better address depression in these diverse groups compared to standard treatments available in the community. Participants in the study are assigned to one of two groups: one receiving the CA-CBT treatment and the other receiving the usual care like counseling services available in schools. The CA-CBT treatment lasts for eight weeks and includes sessions tailored to the cultural backgrounds of the participants, with facilitators who speak the participants' languages. The study measures the effectiveness of the treatment by looking at changes in depression levels before and after the intervention. Results show that those who received CA-CBT had a greater reduction in depressive symptoms and fewer participants dropped out of the program, suggesting the therapy's cultural relevance and engagement. The study supports the use of culturally tailored therapies in school and community settings.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.175 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 13 to 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Adolescents aged 13 to 18 years old * Screening positive for mild to moderate depressive symptoms based on the PHQ-9 * Able to understand and communicate in English, Arabic, or Tagalog * Parental/guardian consent and participant assent provided * Willing to attend all 8 weekly therapy sessions Exclusion Criteria: * Currently undergoing structured psychotherapy or psychiatric treatment * Diagnosed with severe mental disorders (e.g., psychosis, bipolar disorder) * Active suicidal ideation requiring emergency intervention * Significant cognitive or developmental delays that impede participation * Unwilling or unable to commit to full program attendance Exclusion Criteria: \-
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Bath Spa University Academic Centre - Ras Al Khaimah
Ras al-Khaimah, United Arab EmiratesOpen Bath Spa University Academic Centre - Ras Al Khaimah in Google Maps