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RECRUITING
NCT06181643
NA

Innovating CBT-I for Cancer Survivors: An Optimization Trial

Sponsor: Massachusetts General Hospital

View on ClinicalTrials.gov

Summary

The overall goal of this project is to conduct a factorial, randomized controlled trial to optimize synchronous, virtual delivery of CBT-I for cancer survivors. The proposed project will yield multiple deliverables to innovate cancer survivorship care, chiefly an optimized, scalable, virtually-delivered intervention that addresses chronic insomnia, one of the most deleterious concerns among the growing demographic of cancer survivors in the U.S. Findings will inform future considerations for delivering CBT-I to cancer survivors.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2024-09-06

Completion Date

2026-05-31

Last Updated

2026-03-13

Healthy Volunteers

No

Interventions

BEHAVIORAL

Survivorship Sleep Program with Individual Delivery + No Booster Sessions

4 weekly SSP sessions delivered to individual participants (session durations approximately 45 min/session). No booster sessions.

BEHAVIORAL

Survivorship Sleep Program with Group Delivery + No Booster Sessions

4 weekly SSP sessions delivered to groups of participants (session durations approximately 90 min/session). No booster sessions.

BEHAVIORAL

Survivorship Sleep Program with Individual Delivery + 3 Booster Sessions

4 weekly SSP sessions delivered to individual participants (session durations approximately 45 min/session). 3 monthly booster sessions.

BEHAVIORAL

Survivorship Sleep Program with Group Delivery + 3 Booster Sessions

4 weekly SSP sessions delivered to groups of participants (session durations approximately 90 min/session). 3 monthly booster sessions.

Locations (1)

Massachusetts General Hospital

Boston, Massachusetts, United States