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Improving Sleep in Gynecologic Cancer Survivors

NCT05044975 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2026-05-22

No results posted yet for this study

Summary

This purpose of this study is to learn about how to provide treatment to gynecologic cancer survivors who have difficulty sleeping.

Conditions

  • Sleep Disturbance
  • Gynecologic Cancer

Interventions

BEHAVIORAL

Sleep restriction

Participants will receive sleep restriction intervention

BEHAVIORAL

Stimulus control

Participants will receive stimulus control intervention

BEHAVIORAL

Systematic light exposure

Participants will receive systematic light exposure intervention

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • University of Arizona

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-11
Primary Completion
2025-08-07
Completion
2025-08-07

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05044975 on ClinicalTrials.gov