Condition: Breast Cancer · Insomnia · Weight Gain · Sponsor: Johns Hopkins University
The investigators propose a randomized controlled clinical trial in 250 women with a history of early stage breast cancer who are overweight or obese with insomnia to test whether a brief, cognitive-behavioral intervention for insomnia (CBT-I) prior to behavioral weight loss (CBT-I+BWL) is superior to a sleep education control (EDU) condition followed by behavioral weight loss (EDU+BWL). The investigators will measure outcomes at baseline, 8 weeks (after completing CBT-I or EDU and prior to BWL), and at 3, 6, and 12 months.
This description comes directly from the study's public registry record.
Janelle Wilder Coughlin, PHD · (410) 550-7000 · jwilder3@jhmi.edu
Katie Smith, BA · (410) 550-8099 · ksmit261@jhmi.edu
Always discuss trial participation with your own doctor first.
| Sibley Memorial Hospital | Washington D.C., District of Columbia, United States | Recruiting |
| Sidney Kimmel Comprehensive Cancer Center, the Avon Foundation Breast Center at Johns Hopkins | Baltimore, Maryland, United States | Recruiting |
| Johns Hopkins Bayview | Baltimore, Maryland, United States | Recruiting |
| Johns Hopkins Kimmel Cancer Center at Greenspring Station | Lutherville, Maryland, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05780814