NCT07334769

Brief Summary

This study aims to examine the effect of a newly developed religously oriented cognitive behavioral group therapy program on the level of anxiety and well-being in young adults compared to the traditional cognitive behavioral therapy-based program. Hypoteses 1 Religiously oriented CBT group therapy will be more effective in reducing participants' general anxiety levels compared to traditional CBT group therapy and the control group, and this effect will continue in the two-month follow-up measurements. Hypoteses 2 Religiously oriented CBT group therapy will be more effective in increasing participants' levels of well-being compared to traditional CBT group therapy and the control group, and this effect will continue in the two-month follow-up measurements.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
33

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

February 22, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 9, 2024

Completed
12 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 21, 2024

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

December 31, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

January 12, 2026

Completed
Last Updated

January 12, 2026

Status Verified

January 1, 2025

Enrollment Period

7 months

First QC Date

December 31, 2025

Last Update Submit

December 31, 2025

Conditions

Keywords

generalized anxiety disordergroup therapycognitive behavioral group therapywell-being

Outcome Measures

Primary Outcomes (1)

  • Anxiety

    The Anxiety Thoughts Inventory (AnTI) is a self-report measure assessing the frequency of anxiety-related thoughts. The total score is calculated by summing item responses, with higher scores indicating greater levels of maladaptive anxious thinking. Lower scores reflect fewer anxiety-related cognitions and improvement over time. Change in scores from baseline to post-intervention and follow-up represents a reduction in anxiety-related thought patterns.

    Baseline (pre-test), immediately post-intervention (post-test), and 2-month follow-up.

Secondary Outcomes (1)

  • Well-being

    Baseline (pre-test), immediately post-intervention (post-test), and 2-month follow-up.

Study Arms (3)

Traditional Cognitive Behavioral Group Therapy

ACTIVE COMPARATOR

Participants in this group received 10 sessions of online cognitive behavioral group therapy

Behavioral: Traditional Cognitive Behavioral Group Therapy

Waiting Group

OTHER

There is no intervention for this group

Other: Waiting Group

Religiously Integrated Cognitive Behavioral Group Therapy

EXPERIMENTAL

Participants in this group received 10 sessions of online religiously integrated cognitive behavioral group therapy

Behavioral: Religiosly Integrated Cognitive Behavioral GroupTherapy

Interventions

This intervention consists of a structured, group-based, online cognitive behavioral therapy program integrated with participants' spiritual/religious values. The program includes psychoeducation about anxiety, cognitive restructuring, exposure to uncertainty, problem-solving, and behavioral exercises, combined with spiritually framed coping strategies such as meaning-making, patience, gratitude, trust, and values-based reflection. Sessions were delivered weekly in a standardized manualized format by a trained therapist. The intervention aimed to reduce anxiety symptoms and enhance psychological well-being.

Religiously Integrated Cognitive Behavioral Group Therapy

Participants assigned to the waitlist control group did not receive any active intervention during the study period and were offered the intervention after completion of post-test assessments.

Waiting Group

his intervention consists of a structured, group-based, online cognitive behavioral therapy program focusing on anxiety management. The program includes psychoeducation, cognitive restructuring, graduated exposure to anxiety-provoking situations and intolerance of uncertainty, problem-solving, and behavioral exercises. Sessions were delivered weekly in a standardized, manualized format by a trained therapist, without spiritual or religious content.

Traditional Cognitive Behavioral Group Therapy

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Being between 18 and 45 years of age, Willingness to participate in 10 weekly group sessions, Having a GAD-7 score of 5 or higher, Exhibiting symptoms of generalized anxiety disorder as determined by the Structured Clinical Interview for DSM-5 (SCID-5-CV), Having regular access to the internet.

You may not qualify if:

  • Currently receiving any form of psychological treatment Having previously undergone long-term psychotherapy Having a primary comorbid psychological disorder other than generalized anxiety disorder, Expressing suicidal ideation, Having completed only primary school education

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

İstanbul

Istanbul, Türkiye, 34000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety DisordersPanic DisorderGeneralized Anxiety Disorder

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Ekinci, PhD Candidate

    Ibn Haldun University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
This study is open-label. Due to the nature of the psychological group interventions, neither participants nor therapists could be blinded to treatment allocation. Outcome measures were based on self-report scales.
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Psychologist

Study Record Dates

First Submitted

December 31, 2025

First Posted

January 12, 2026

Study Start

February 22, 2024

Primary Completion

September 9, 2024

Study Completion

September 21, 2024

Last Updated

January 12, 2026

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL, SAP
Time Frame
Individual participant data (IPD) will be made available beginning 6 months after publication of the primary study results and will remain available for a period of 5 years.

Locations