Breast Cancer Clinical Trial

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Feasibility and Effectiveness of a Sleep Hygiene Education Program for Sleep Issues in Breast Cancer Survivors

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Summary

The proposed research will assess the feasibility and preliminary effectiveness of a Sleep Hygiene Program for Breast Cancer Survivors. Participants will complete assessments related to sleep issues, participate in a Sleep Hygiene Program, and complete another assessment post-intervention.

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Eligibility Criteria

Inclusion Criteria:

diagnosed with breast cancer and not currently receiving active treatment in the form of chemotherapy or radiation therapy,
at least 18 years of age,
women
score > 5 on the Pittsburgh Sleep Quality Index
Participant has a smartphone that operates on the Android or Apple platform
Participant is able to use the Ecological Momentary Assessment application in the morning
functional English fluency and literacy

Exclusion Criteria:

self-reported history of diagnosis of co-morbidities that have been associated with poor sleep and fatigue: chronic insomnia, chronic fatigue syndrome, unstable heart, lung, or neuromuscular disease, insulin-dependent diabetes, sleep apnea, chronic oral steroid therapy, and night-shift employment.
Currently taking a pharmacological sleep aide

Study is for people with:

Breast Cancer

Study ID:

NCT04232319

Recruitment Status:

Withdrawn

Sponsor:

University of Toledo Health Science Campus

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There is 1 Location for this study

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University of Toledo
Toledo Ohio, 43606, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT04232319

Recruitment Status:

Withdrawn

Sponsor:


University of Toledo Health Science Campus

How clear is this clinincal trial information?

Clinical Trial Resources

SurvivorNet’s Guide To Clinical Trials: What Are They And Are They Right for You?
Clinical Trials for Breast Cancer
Have You Been Diagnosed With Late-Stage Breast Cancer? Know That You Have Treatment Options.
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