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NOT YET RECRUITING
NCT07835698
NA

The Validation of ICBT Clinical Trial: Disease Stress Adjustment in Breast Cancer Patients

Sponsor: National Health Research Institutes, Taiwan

View on ClinicalTrials.gov

Summary

Breast cancer and its treatment can cause ongoing emotional distress, including anxiety, depressive symptoms, stress-related reactions, and difficulties adjusting to life after treatment. This study evaluates an 8-week Internet-based cognitive behavioral therapy (ICBT) program designed to support psychological adjustment and improve quality of life among adults with stage I-III breast cancer who have completed primary cancer treatment. Approximately 100 participants will be randomly assigned to either an ICBT group or a control group. Participants in the ICBT group will receive treatment as usual together with the 8-week online program, while participants in the control group will receive treatment as usual alone during the main study period. The study will compare changes in anxiety, depressive symptoms, post-traumatic stress symptoms, and quality of life between the two groups.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-10-01

Completion Date

2027-08-21

Last Updated

2026-09-23

Healthy Volunteers

No

Interventions

BEHAVIORAL

Internet-Based Cognitive Behavioral Therapy Program for Breast Cancer Survivors

An 8-week Internet-based cognitive behavioral therapy program delivered through a mobile application. The program includes psychoeducational content and exercises related to self-compassion, cognitive restructuring, emotional regulation, stress management, relaxation, mindfulness, and coping with cancer-related concerns.

OTHER

Treatment as Usual (TAU)

Participants will continue to receive routine clinical care provided by their treating health care professionals. No additional Internet-based cognitive behavioral therapy will be provided during the main comparative study period.