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The Better Sleep for Supporters With Insomnia Study (BeSSI)

Primary Purpose

Family Caregivers, Cancer, Insomnia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SHUTi (Sleep Healthy Using the Internet)
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Family Caregivers focused on measuring Family Caregivers, Cancer, Insomnia

Eligibility Criteria

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

Inclusion Criteria:

  • self-report providing unpaid care (e.g., practical, medical, and/or emotional support) to an adult family member or "family-like" close individual who is either currently undergoing any anti-cancer treatment (e.g., surgery, chemotherapy, radiation, for either curative or palliative intent) or has completed anti-cancer treatment within the past 2 years.
  • Insomnia severity index score of 10 or higher
  • age 18 and over
  • regular access (at least 2/week) and willingness to use a computer and the Internet and check email
  • ability to read and speak English
  • resident of the US

Exclusion Criteria:

  • irregular sleep schedules that prevent the ability to follow intervention recommendations (i.e., with usual bedtimes outside of 8:00pm to 2:00am or arising time outside of 4:00am to 10:00am)
  • current psychological treatment for insomnia
  • screen positive for a history of psychotic or bipolar disorder; and current severe depression, high risk of suicide, substance use (alcohol, drug) disorder within the past year
  • symptoms suggestive of untreated sleep disorders other than insomnia (e.g., obstructive sleep apnea, restless legs syndrome, periodic limb movement disorder)
  • presence of uncontrolled medical condition that is deemed to interfere with the study procedures, or put the study participant at undue risk
  • Unstable medication regimen (change to schedule or dosage within past 3 months) for a prescription medication regimen thought to impact sleep.

Sites / Locations

  • University of Virginia

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SHUTi

Arm Description

Outcomes

Primary Outcome Measures

SHUTi Usage
Number of SHUTi Cores completed by participants

Secondary Outcome Measures

Insomnia severity
Insomnia severity index; 7 items; summed scores range from 0 to 28 (higher scores indicate more severe insomnia symptoms)
Sleep onset latency (SOL)
Data collected from sleep diary: Time fell asleep - Time attempting to fall asleep
Wake after sleep onset (WASO)
Data collected from sleep diary: Total time awake between time feel asleep and final morning waking
Perceived sleep quality
Data collected from sleep diary: Nightly rating of perceived sleep quality from very poor to very good
Sleep-related cognitions
Dysfunctional Beliefs and Attitudes about Sleep; 16 items; averaged scores range from 0 to 10 (higher scores indicate more dysfunctional attitudes and beliefs about sleep)
Sleep self-efficacy
Sleep Self-Efficacy Scale; 13-items; averaged scores range from 0 to 10 (higher scores indicate greater self-efficacy)
Internal and chance sleep locus of control
Sleep Locus of Control Scale; 4-item subscales for internal and chance locus of control, respectively; averaged scores per scale range from 1 to 6 (higher scores indicate higher belief in the locus of control measured)
Caregiving burden
Pearlin Stress Scale - Overload subscale; 4 items; averaged scores range from 1 to 4 (higher scores indicate greater perceived burden)
Caregiving competence
Pearlin Stress Scale - Caregiving Competence subscale; 4 items; averaged scores range from 1 to 4 (higher scores indicate greater perceived competence)
Physical Function
PROMIS SF v2.0 - Physical Function 8b; 8 items; scored on a normalized T-score distribution (higher scores indicate higher physical function)
Anxiety
PROMIS SF v2.0 - Anxiety 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher anxiety)
Depression
PROMIS SF v2.0 - Depression 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher depression)
Fatigue
PROMIS SF v2.0 - Fatigue 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher fatigue)
Sleep Disturbance
PROMIS SF v2.0 - Sleep Disturbance 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher sleep disturbance)
Social functioning
PROMIS SF v2.0 - Ability to Participant in Social Roles and Activities 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher social function)
Pain Interference
PROMIS SF v2.0 - Pain Interference 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher pain interference)
Pain Intensity
PROMIS SF v2.0 - Pain Intensity item; 1 item (higher score indicate higher pain intensity)
Experiences with Internet intervention
Internet Intervention Utility Questionnaire (UQ) for SHUTi; 18 items; items examined individually
Perceptions of Internet intervention
Internet Intervention Impact and Effectiveness Questionnaire (IEQ) for SHUTi; 29 items; items examined individually
Adherence to Internet intervention
Internet Intervention Adherence Questionnaire (AQ) for SHUTi; 20 items; items examined individually
SHUTi Feasibility as assessed by open-ended feedback
Open-ended survey items regarding barriers to using SHUTi
SHUTi Acceptability as assessed by open-ended feedback
Open-ended survey items regarding appropriateness of SHUTi to address caregivers' sleep needs

Full Information

First Posted
October 28, 2020
Last Updated
May 16, 2022
Sponsor
University of Virginia
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1. Study Identification

Unique Protocol Identification Number
NCT04661306
Brief Title
The Better Sleep for Supporters With Insomnia Study
Acronym
BeSSI
Official Title
Optimizing Efficiency and Impact of Internet-delivered Insomnia Treatment for Cancer Caregivers
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
September 30, 2020 (Actual)
Primary Completion Date
January 31, 2022 (Actual)
Study Completion Date
January 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will identify whether - and if so, how - tailoring would increase adoption of and benefit from an interactive internet intervention for insomnia called SHUTi (Sleep Healthy Using the Internet) for cancer caregivers. Participating caregivers' sleep and sleep-related characteristics will be characterized from a baseline assessment; then, caregivers will receive complementary and voluntary access to SHUTi. Among caregivers who choose to use SHUTi, intervention use, perceived appropriateness, and effects on sleep and quality of life will be assessed. Among caregivers who choose not to use SHUTi, reasons and barriers to using the intervention will be assessed.
Detailed Description
Insomnia is a significant public health problem with substantial medical, psychological and financial ramifications. About 50-75% of the 3.5 million Americans who provide unpaid medical, practical, and/or emotional support for a loved one with cancer endorse clinically significant sleep disturbance. Understanding caregivers' psychosocial risk factors and needs, and the extent to which these are unique to the cancer caregiving context, will ensure appropriate and effective interventions for cancer caregivers with insomnia. Existing psychosocial services for caregivers are primarily delivered in-person. Although such interventions are effective, they suffer from low enrollment, high dropout, and limited reach to caregivers who already have inadequate healthcare access, like caregivers from lower SES or those in rural areas. Digital health interventions can lower barriers to entry to supportive care for caregivers as they are conveniently accessible anywhere and anytime from an Internet-enabled device. Sleep Healthy Using the Internet (SHUTi) is a NCI-designated research-tested intervention that delivers cognitive-behavioral therapy for insomnia (CBT-I) and holds significant potential to accessibly treat insomnia for cancer caregivers. Most digital health interventions tested among caregivers, however, have been developed de novo for specific caregiving contexts. The implicit assumption underlying highly tailored interventions for caregivers is that caregivers have different deficits, risk factors, and needs from non-caregivers. This assumption has not often been tested, and therefore the extent to which caregivers want and need tailoring for digital health interventions is not known. This study is therefore designed to provide the data necessary to ensure the highest quality, impact, and efficiency from existing evidence-based digital health interventions to meet pressing psychosocial needs among cancer caregivers. Specifically, this study will directly inform next research steps for tailoring and testing SHUTi for optimal impact and reach among caregivers. The SHUTi Program: SHUTi is a self-guided (i.e., automated), interactive, and tailored web-based program modeled on the primary tenants of face-to-face CBT-I (sleep restriction, stimulus control, cognitive restructuring, sleep hygiene, relapse prevention). Intervention content is metered out over time through 6 "Cores." Users obtain access to a new Core based on a time and event-based schedule (e.g., 7 days after completion of previous Core). This schedule is consistent with the recommendation from a task force commissioned by the Academy of Sleep Medicine, which deemed that an average of 6 - 8 sessions constitutes "adequate treatment exposure". The SHUTi program relies on user-entered online Sleep Diaries to track progress and to tailor treatment recommendations (i.e., assign a "sleep restriction" window). Each Core acts as an online analog for the weekly sessions typically used when delivering CBT-I in a face-to-face format, following the same general structure: 1) Core objectives (what will be learned and why this information is important), 2) review of previous week's homework and sleep diary data, 3) new intervention material, 4) assignment of homework (treatment strategies for the coming week), and 5) a summary of the Core's main points. Intervention content is enhanced through a variety of interactive features, including personalized goal-setting, graphical feedback based on inputted symptoms, animations / illustrations to enhance comprehension, quizzes to test user knowledge, patient vignettes, and video-based expert explanation. Automated emails are also sent to encourage program adherence. There is no content that is specifically about cancer or caregiving. Caregivers participating in this study will complete a baseline assessment (questionnaires and 2 weeks of daily sleep diaries), and then will receive complementary and voluntary access to SHUTi. Participants who choose to complete 1 or more SHUTi Cores will complete a follow-up assessment of questionnaires and 2 weeks of sleep diaries; participants who choose not to complete any SHUTi cores will be asked to provide brief feedback regarding their reasons/barriers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Family Caregivers, Cancer, Insomnia, Sleep Initiation and Maintenance Disorders
Keywords
Family Caregivers, Cancer, Insomnia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
SHUTi
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
SHUTi (Sleep Healthy Using the Internet)
Other Intervention Name(s)
CBTi
Intervention Description
Cognitive Behavioral Therapy for insomnia delivered online and metered out over 6 weeks in a fully automated, interactive, tailored web-based program
Primary Outcome Measure Information:
Title
SHUTi Usage
Description
Number of SHUTi Cores completed by participants
Time Frame
9 weeks
Secondary Outcome Measure Information:
Title
Insomnia severity
Description
Insomnia severity index; 7 items; summed scores range from 0 to 28 (higher scores indicate more severe insomnia symptoms)
Time Frame
Baseline, 9 weeks
Title
Sleep onset latency (SOL)
Description
Data collected from sleep diary: Time fell asleep - Time attempting to fall asleep
Time Frame
Baseline, 9 weeks
Title
Wake after sleep onset (WASO)
Description
Data collected from sleep diary: Total time awake between time feel asleep and final morning waking
Time Frame
Baseline, 9 weeks
Title
Perceived sleep quality
Description
Data collected from sleep diary: Nightly rating of perceived sleep quality from very poor to very good
Time Frame
Baseline, 9 weeks
Title
Sleep-related cognitions
Description
Dysfunctional Beliefs and Attitudes about Sleep; 16 items; averaged scores range from 0 to 10 (higher scores indicate more dysfunctional attitudes and beliefs about sleep)
Time Frame
Baseline, 9 weeks
Title
Sleep self-efficacy
Description
Sleep Self-Efficacy Scale; 13-items; averaged scores range from 0 to 10 (higher scores indicate greater self-efficacy)
Time Frame
Baseline, 9 weeks
Title
Internal and chance sleep locus of control
Description
Sleep Locus of Control Scale; 4-item subscales for internal and chance locus of control, respectively; averaged scores per scale range from 1 to 6 (higher scores indicate higher belief in the locus of control measured)
Time Frame
Baseline, 9 weeks
Title
Caregiving burden
Description
Pearlin Stress Scale - Overload subscale; 4 items; averaged scores range from 1 to 4 (higher scores indicate greater perceived burden)
Time Frame
Baseline, 9 weeks
Title
Caregiving competence
Description
Pearlin Stress Scale - Caregiving Competence subscale; 4 items; averaged scores range from 1 to 4 (higher scores indicate greater perceived competence)
Time Frame
Baseline, 9 weeks
Title
Physical Function
Description
PROMIS SF v2.0 - Physical Function 8b; 8 items; scored on a normalized T-score distribution (higher scores indicate higher physical function)
Time Frame
Baseline, 9 weeks
Title
Anxiety
Description
PROMIS SF v2.0 - Anxiety 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher anxiety)
Time Frame
Baseline, 9 weeks
Title
Depression
Description
PROMIS SF v2.0 - Depression 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher depression)
Time Frame
Baseline, 9 weeks
Title
Fatigue
Description
PROMIS SF v2.0 - Fatigue 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher fatigue)
Time Frame
Baseline, 9 weeks
Title
Sleep Disturbance
Description
PROMIS SF v2.0 - Sleep Disturbance 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher sleep disturbance)
Time Frame
Baseline, 9 weeks
Title
Social functioning
Description
PROMIS SF v2.0 - Ability to Participant in Social Roles and Activities 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher social function)
Time Frame
Baseline, 9 weeks
Title
Pain Interference
Description
PROMIS SF v2.0 - Pain Interference 8a; 8 items; scored on a normalized T-score distribution (higher scores indicate higher pain interference)
Time Frame
Baseline, 9 weeks
Title
Pain Intensity
Description
PROMIS SF v2.0 - Pain Intensity item; 1 item (higher score indicate higher pain intensity)
Time Frame
Baseline, 9 weeks
Title
Experiences with Internet intervention
Description
Internet Intervention Utility Questionnaire (UQ) for SHUTi; 18 items; items examined individually
Time Frame
9 weeks
Title
Perceptions of Internet intervention
Description
Internet Intervention Impact and Effectiveness Questionnaire (IEQ) for SHUTi; 29 items; items examined individually
Time Frame
9 weeks
Title
Adherence to Internet intervention
Description
Internet Intervention Adherence Questionnaire (AQ) for SHUTi; 20 items; items examined individually
Time Frame
9 weeks
Title
SHUTi Feasibility as assessed by open-ended feedback
Description
Open-ended survey items regarding barriers to using SHUTi
Time Frame
9 weeks
Title
SHUTi Acceptability as assessed by open-ended feedback
Description
Open-ended survey items regarding appropriateness of SHUTi to address caregivers' sleep needs
Time Frame
9 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: self-report providing unpaid care (e.g., practical, medical, and/or emotional support) to an adult family member or "family-like" close individual who is either currently undergoing any anti-cancer treatment (e.g., surgery, chemotherapy, radiation, for either curative or palliative intent) or has completed anti-cancer treatment within the past 2 years. Insomnia severity index score of 10 or higher age 18 and over regular access (at least 2/week) and willingness to use a computer and the Internet and check email ability to read and speak English resident of the US Exclusion Criteria: irregular sleep schedules that prevent the ability to follow intervention recommendations (i.e., with usual bedtimes outside of 8:00pm to 2:00am or arising time outside of 4:00am to 10:00am) current psychological treatment for insomnia screen positive for a history of psychotic or bipolar disorder; and current severe depression, high risk of suicide, substance use (alcohol, drug) disorder within the past year symptoms suggestive of untreated sleep disorders other than insomnia (e.g., obstructive sleep apnea, restless legs syndrome, periodic limb movement disorder) presence of uncontrolled medical condition that is deemed to interfere with the study procedures, or put the study participant at undue risk Unstable medication regimen (change to schedule or dosage within past 3 months) for a prescription medication regimen thought to impact sleep.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kelly Shaffer, PhD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22903
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27902836
Citation
Ritterband LM, Thorndike FP, Ingersoll KS, Lord HR, Gonder-Frederick L, Frederick C, Quigg MS, Cohn WF, Morin CM. Effect of a Web-Based Cognitive Behavior Therapy for Insomnia Intervention With 1-Year Follow-up: A Randomized Clinical Trial. JAMA Psychiatry. 2017 Jan 1;74(1):68-75. doi: 10.1001/jamapsychiatry.2016.3249.
Results Reference
background
PubMed Identifier
30245560
Citation
Shaffer KM, Garland SN, Mao JJ, Applebaum AJ. Insomnia among Cancer Caregivers: A Proposal for Tailored Cognitive Behavioral Therapy. J Psychother Integr. 2018 Sep;28(3):275-291. doi: 10.1037/int0000105.
Results Reference
background
Links:
URL
https://med.virginia.edu/bht/
Description
Center for Behavioral Health and Technology website

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The Better Sleep for Supporters With Insomnia Study

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