Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
NCT07119515

Teletherapy vs. In-Person Cognitive Behavioral Therapy for Generalized Anxiety Disorder

Led by Government College University Faisalabad · Updated on 2025-08-13

25

Participants Needed

1

Research Sites

24 weeks

Total Duration

On this page

Sponsors

G

Government College University Faisalabad

Lead Sponsor

A

Allied Hospital Faisalabad

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this randomized controlled trial is to compare the clinical efficacy of teletherapy versus in-person third-wave cognitive behavioral therapy (CBT) in treating generalized anxiety disorder (GAD) among young individuals aged 18-45 years in Pakistan. The main questions it aims to answer are: * Is teletherapy as effective as in-person therapy in reducing anxiety symptoms and stress? * Do therapeutic alliance, treatment adherence, and social support influence treatment outcomes differently across delivery methods? Researchers will compare the teletherapy group (remote sessions via digital platforms) and the in-person therapy group (face-to-face sessions) to evaluate differences in symptom reduction, general health improvement, and moderating factors like therapeutic alliance. Participants will: * Undergo a 8-week intervention with weekly structured third-wave CBT sessions. * Complete assessments at baseline, post-intervention, and follow-up using validated scales (e.g., Generalized Anxiety Disorder-7 \[GAD-7\], Hamilton Anxiety Rating Scale \[HAM-A\]). * Engage in modules including mindfulness, behavioral activation, and exposure therapy, adapted for their assigned delivery method. This study aims to address gaps in mental health accessibility in Pakistan by evaluating whether teletherapy can serve as a viable alternative to traditional in-person care.

CONDITIONS

Official Title

Teletherapy vs. In-Person Cognitive Behavioral Therapy for Generalized Anxiety Disorder

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 45 years
  • Diagnosis of generalized anxiety disorder according to DSM-5 TR criteria
  • Ability to understand and read English
  • Ability to use digital technology and have access to the Internet
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Presence of risk of suicide or self-destructive behaviors
  • Having another severe mental disorder such as substance abuse, psychotic disorder, or bipolar disorder
  • Presence of severe personality disorder
  • Having a medical condition that prevents participation in treatment
  • Receiving another psychological treatment during the study
  • Increase or change in medication during the study period

AI-Screening

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Trial Site Locations

Total: 1 location

1

Allied Hospital II

Faisalabad, Punjab Province, Pakistan, 38000

Actively Recruiting

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Research Team

I

imaan Sabeeh, MS Scholar

CONTACT

A

Asma Riaz, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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