Feasibility of Internet Group CBT-I for Gyn Oncology Patients

a study on Insomnia Sleep Disorders Cognitive Behavioral Therapy

Summary

Eligibility
for females ages 18 years and up (full criteria)
Location
at UC Davis
Dates
study started
completion around
Principal Investigator
by Hui Chen (ucdavis)

Description

Summary

The goal of this study is to evaluate the feasibility and acceptability of delivering cognitive behavioral therapy for insomnia (CBT-I) to gynecologic cancer patients in an internet-based small-group setting.

Secondary objectives:

  1. To compare insomnia symptoms before and after intervention.
  2. To evaluate any changes in quality of life symptoms while undergoing the intervention.
  3. To evaluate the duration of symptoms improvement after the intervention is complete.

Official Title

Feasibility of Internet-Delivered Group Cognitive Behavioral Therapy for Insomnia in Gynecologic Oncology Patients

Details

This is a pilot feasibility study looking at delivering CBT-I to gynecologic cancer patients. This study will be completed via a novel internet based small group platform. Twelve eligible participants will meet weekly for 6 weeks while undergoing the CBT-I program.

Keywords

Insomnia, Sleep Initiation and Maintenance Disorders, Cognitive Behavioral Therapy for Insomnia

Eligibility

You can join if…

Open to females ages 18 years and up

  1. English-speaking women greater than 18 years old who present to UC Davis Comprehensive Cancer Center for treatment or surveillance of gynecologic cancer
  2. Must have access to internet
  3. Be able to connect via secure web-based platform
  4. Be able to complete online questionnaires
  5. Moderate or severe insomnia
  6. Have access to a mobile device or computer

You CAN'T join if...

  1. Participants without ability to connect with both audio and visual through secure web-based platform
  2. Participant is currently taking sleep medication prescribed by their provider for sleep disturbance or insomnia - Patients taking over the counter medications or supplements are eligible
  3. Participants with remote history of insomnia, but not currently having symptoms of insomnia
  4. Have other reasons for poor sleep

Location

  • University of California, Davis Comprehensive Cancer Center accepting new patients
    Sacramento California 95817 United States

Lead Scientist at University of California Health

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Davis
ID
NCT06060158
Study Type
Interventional
Participants
Expecting 12 study participants
Last Updated