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Digital Cognitive Behavioral Therapy for Insomnia (dCBT-I) for Chronic Insomnia in Breast Cancer Survivors, A Randomized Controlled Trial
To explore the efficacy of dCBT-I therapy for chronic insomnia among breast cancer survivors in China, we propose to conduct a randomized, parallel controlled clinical study in breast cancer survivors using a smartphone Chinese application (app) "resleep". Breast cancer survivors with chronic insomnia were recruited from our Breast Disease Center and externally, with the waiting group as a parallel control and the dCBT-I treatment group as an intervention group, in a 1:1 sample size. Intervention group (dCBT-I treatment group) will receive full self-help dCBT-I administered by smartphone APP for 6 weeks. The control group (waiting for treatment group) will not receive any additional interventions based on the original conventional treatment and will be followed up as planned, waiting for treatment.At the end of the 3-month follow-up, the decision to receive treatment was made according to the patient's wishes. The primary endpoint was the insomnia severity index (ISI) at the end of treatment and at 3 months of treatment.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Jing Ma
Beijing, Beijing Municipality, China
Start Date
August 29, 2023
Primary Completion Date
August 29, 2025
Completion Date
August 29, 2026
Last Updated
October 22, 2024
264
ESTIMATED participants
Digital Cognitive Behavioral Therapy for Insomnia
BEHAVIORAL
Lead Sponsor
Peking University First Hospital
Collaborators
NCT07429578
NCT06968013
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT04471168