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CBT-I Intervention for Insomnia in Newly Diagnosed Cancer Patients

Primary Purpose

Cancer, Chronic Insomnia

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
cognitive behavioral therapy for insomnia (CBTI)
Waitlist control condition
Sponsored by
Virginia Commonwealth University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer focused on measuring insomnia, Sleep, CBT-I intervention, SHUTi

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • newly diagnosed with I-III non-metastatic cancer
  • scheduled to begin chemotherapy or radiotherapy
  • chemotherapy or radiotherapynaïve
  • meet diagnostic criteria for chronic insomnia (i.e., lasting for at least one month)
  • Chronic insomnia has been defined in previous research:as the presence of (1) three or more episodes of insomnia (i.e., ≥ 30minuteSOL, ≥ 60minute wake after sleep onset (WASO), or ≤ 6.5 hour total sleep time (TST) per night) of per week and (2) daytime effects of insomnia, such as irritability, difficulty concentrating, or fatigue for at least one month.
  • interested in behavioral sleep treatment
  • have the permission of their oncologists to participate.

Exclusion criteria:

  • untreated alcohol or substance abuse or dependence, bipolar, or psychotic disorder
  • medical conditions such as seizure disorder, restless leg disorder, or Parkinson's disease
  • untreated sleep disorders such as sleep apnea

Sites / Locations

  • Virginia Commonwealth University/Massey Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

CBTI treatment

Waitlist control condition

Arm Description

cognitive behavioral therapy for insomnia (CBTI) treatment is a validated web based version of CBT-I, which will take place over seven weeks and will include a combination of face-to-face and telephone sessions, and email updates

No advice regarding sleep will be given to the control group and if participants ask, they will be informed that such advice can be provided in a few weeks if they choose to crossover to the treatment condition at the end of the study.

Outcomes

Primary Outcome Measures

To determine the efficacy of a CBT-I intervention that improves sleep and quality of life outcomes during cancer treatment.
CBT-I is a cognitive behavioral therapy for insomnia. Pretreatment,all participants will complete a two week sleep diary and multiple self report measures. At the end of the intervention, all participants will complete a two week sleep diary and multiple self report measures again.

Secondary Outcome Measures

To assess the feasibility of a CBT--I intervention among newly diagnosed cancer patients.
To assess the acceptability of a CBT--I intervention among newly diagnosed cancer patients.

Full Information

First Posted
March 11, 2015
Last Updated
February 9, 2016
Sponsor
Virginia Commonwealth University
Collaborators
Massey Cancer Center
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1. Study Identification

Unique Protocol Identification Number
NCT02410564
Brief Title
CBT-I Intervention for Insomnia in Newly Diagnosed Cancer Patients
Official Title
Testing an Accessible Cognitive Behavioral Therapy for Insomnia (CBT-I) Intervention in Newly Diagnosed Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Why Stopped
insufficient staff
Study Start Date
December 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Virginia Commonwealth University
Collaborators
Massey Cancer Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To determine the efficacy of a CBT-I intervention in improving sleep and other quality of life outcomes during cancer treatment. To assess the feasibility and acceptability of a CBT-I intervention among newly diagnosed cancer patients.
Detailed Description
The proposed study will be a randomized controlled trial design. Participants will be randomized to either a CBTI treatment or a wait list control condition. The intervention is SHUTi, a validated web based version of CBTI, which will take place over seven weeks and will include a combination of face to face and telephone sessions, and email updates. All participants will have a face to face meeting with the doctoral student at enrollment. During the intervention period, all participants will be contacted by telephone at week 1, 3, and 6 to check in and to encourage participant engagement. However, during phone calls with control participants, no advice regarding sleep will be given and if participants ask, they will be informed that such advice can be provided in a few weeks if they choose to crossover to the treatment condition at the end of the study. Participants in SHUTi will additionally be provided the the doctoral student's phone number and will be encouraged to contact her if they have any questions during the intervention. They will also have the option of setting up appointments for face to face meetings during a clinic appointment if they desire additional therapist guidance. Pretreatment, all participants will complete a two week sleep diary and multiple self report measures. At the end of the intervention, all participants will complete a two week sleep diary and multiple self report measures again.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Chronic Insomnia
Keywords
insomnia, Sleep, CBT-I intervention, SHUTi

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CBTI treatment
Arm Type
Active Comparator
Arm Description
cognitive behavioral therapy for insomnia (CBTI) treatment is a validated web based version of CBT-I, which will take place over seven weeks and will include a combination of face-to-face and telephone sessions, and email updates
Arm Title
Waitlist control condition
Arm Type
Placebo Comparator
Arm Description
No advice regarding sleep will be given to the control group and if participants ask, they will be informed that such advice can be provided in a few weeks if they choose to crossover to the treatment condition at the end of the study.
Intervention Type
Behavioral
Intervention Name(s)
cognitive behavioral therapy for insomnia (CBTI)
Other Intervention Name(s)
SHUTi
Intervention Description
SHUTi program is made up of six, weekly treatment Cores modeled after weekly facetoface(CBTI). Each Core begins by providing a rationale for learning the material, explains main content, homework page with suggestions for improving sleep, and a summarized review of main points. The main content each Core addresses myths about sleep, indepth information about topics, vignettes, and quizzes to evaluate users learning in an interactive. As well as being interactive, SHUTi allows for personalization.Modifications are made to sleep recommendations based in sleep diary data and individually set treatment goals. The cores include Overview, Sleep Behavior Core, Sleep Behavior Core 2, Sleep Education Core, Sleep Thoughts Core, and Problem Prevention Core. Each Core takes approximately 45 to 60 minutes to complete. Cores are presented one at a time; next Core becomes available to users a week after they complete one Core.
Intervention Type
Behavioral
Intervention Name(s)
Waitlist control condition
Other Intervention Name(s)
control
Intervention Description
Phone calls with control participants, no advice regarding sleep will be given and if participants ask, they will be informed that such advice can be provided in a few weeks if they choose to crossover to the treatment condition at the end of the study.
Primary Outcome Measure Information:
Title
To determine the efficacy of a CBT-I intervention that improves sleep and quality of life outcomes during cancer treatment.
Description
CBT-I is a cognitive behavioral therapy for insomnia. Pretreatment,all participants will complete a two week sleep diary and multiple self report measures. At the end of the intervention, all participants will complete a two week sleep diary and multiple self report measures again.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
To assess the feasibility of a CBT--I intervention among newly diagnosed cancer patients.
Time Frame
1 year
Title
To assess the acceptability of a CBT--I intervention among newly diagnosed cancer patients.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: newly diagnosed with I-III non-metastatic cancer scheduled to begin chemotherapy or radiotherapy chemotherapy or radiotherapynaïve meet diagnostic criteria for chronic insomnia (i.e., lasting for at least one month) Chronic insomnia has been defined in previous research:as the presence of (1) three or more episodes of insomnia (i.e., ≥ 30minuteSOL, ≥ 60minute wake after sleep onset (WASO), or ≤ 6.5 hour total sleep time (TST) per night) of per week and (2) daytime effects of insomnia, such as irritability, difficulty concentrating, or fatigue for at least one month. interested in behavioral sleep treatment have the permission of their oncologists to participate. Exclusion criteria: untreated alcohol or substance abuse or dependence, bipolar, or psychotic disorder medical conditions such as seizure disorder, restless leg disorder, or Parkinson's disease untreated sleep disorders such as sleep apnea
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruce Rybarczyk, PhD
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Virginia Commonwealth University/Massey Cancer Center
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States

12. IPD Sharing Statement

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CBT-I Intervention for Insomnia in Newly Diagnosed Cancer Patients

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