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Optimizing Efficiency and Impact of Digital Health Interventions for Caregivers

Primary Purpose

Family Caregivers, Insomnia, Sleep Initiation and Maintenance Disorders

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

Eligibility Criteria

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

Inclusion Criteria:

  • Self-report providing high-intensity unpaid care (e.g., practical, medical, and/or emotional support) to a family member or "family-like" close individual, operationalized as a function of time spent caregiving and care task involvement.
  • Self-report expecting to continue provide high-intensity care for at least another 3 months.
  • Have access to any Internet-enabled device (computer, tablet, smartphone) and willing to be emailed about the study.
  • Insomnia severity index score >= 10
  • Residing in the United States or U.S. territory
  • English literacy

Exclusion Criteria:

  • Unusual average bed/wake times, including for shift work
  • Current behavioral/psych treatment for insomnia
  • Medical contraindication (Restless Leg Syndrome/Periodic Limb Movement Disorder, Obstructive Sleep Apnea, narcolepsy, parasomnia, dementia, Parkinson's, Huntington's, stroke, traumatic brain injury, brain infection/tumor, pregnancy/breastfeeding, hyperthyroidism, cancer, severe respiratory disease, epilepsy)
  • Psychiatric contraindications (mania/hypomania, alcohol or substance abuse/dependence)
  • Changes to prescription medications in the past 3 months (sleep, steroid, amphetamine, other wake-promoting)
  • Severe computer literacy challenges

Sites / Locations

  • University of Pittsburgh
  • University of Virginia

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SHUTi (Sleep Healthy Using the Internet)

Arm Description

Participants will be assigned to the SHUTi (Sleep Healthy Using the Internet) online intervention. They will spend 1-2 hours each week for 6-9 weeks completing daily sleep diaries as well as interactive core content covering topics of sleep behaviors, sleep thoughts, sleep education, and relapse prevention. As users progress through the intervention, they will receive automated, tailored instructions for how to improve their sleep.

Outcomes

Primary Outcome Measures

SHUTi engagement
Level of SHUTi engagement: Core completion (i.e., nonuser [no cores completed], incomplete user [1-3 Cores], or complete user [4-6 Cores])

Secondary Outcome Measures

Open-ended feedback on SHUTi
Non-users' post-assessment will include an open-ended survey regarding barriers to SHUTi adoption, the extent to which barriers were related to caregiving, and what modifications may have increased their motivation to try SHUTi. Users' (i.e., incomplete and complete) post-assessment will include an open-ended survey assessing SHUTi usage barriers and motivations, the extent to which these were related to caregiving, and how tailoring may improve usage by increasing salience to caregivers.
SHUTi evaluation
Items from the Internet Intervention Utility, Evaluation, and Adherence questionnaire assess users' perceived usability, acceptability, and perceived efficacy of SHUTi as well as barriers to program use
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 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)

Full Information

First Posted
July 16, 2021
Last Updated
October 2, 2023
Sponsor
University of Virginia
Collaborators
University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT04986904
Brief Title
Optimizing Efficiency and Impact of Digital Health Interventions for Caregivers
Official Title
Optimizing Efficiency and Impact of Digital Health Interventions for Caregivers: A Mixed Methods Approach
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
January 11, 2022 (Actual)
Primary Completion Date
March 6, 2023 (Actual)
Study Completion Date
March 19, 2023 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

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

5. Study Description

Brief Summary
The overall objective of this mixed-methods proposal is to answer the focused research question: What tailoring is necessary and sufficient to achieve optimal engagement with and efficacy of Sleep Healthy Using the Internet (SHUTi) for caregivers? The SHUTi program is a fully-automated Internet-delivered cognitive-behavioral therapy for insomnia (CBT-I) program. We will identify caregiving-related user- and environment characteristics that affect the use and impact of SHUTi, and other Internet interventions more broadly, for caregivers. We will recruit 100 high-intensity caregivers with insomnia to complete a baseline assessment of insomnia and caregiving context. Caregivers will then receive access to SHUTi in an open-label trial. At the end of the 9-week intervention period, caregivers will complete post-assessment and be categorized according to their level of engagement with the 6 SHUTi intervention lessons (or weekly "Cores"). We will test whether caregivers' engagement with SHUTi (i.e., being a non-user vs. incomplete user vs. complete user) is associated with their caregiving-related user characteristics (i.e., caregiving strain, self-efficacy, and guilt) and environment characteristics (i.e., proximity to care recipient; care recipient functional, cognitive, and behavioral status; caregiving tasks). Caregivers' barriers to and motivations for SHUTi engagement will be described from open-ended survey responses specific to participants' level of engagement as part of post-assessment. We will identify non-users' barriers to SHUTi adoption, the extent to which barriers were related to caregiving, and what modifications may have increased their motivation to try SHUTi. We will also identify users' (incomplete and complete) SHUTi usage barriers and motivations, the extent to which these were related to caregiving, and how tailoring may improve usage by increasing salience to caregivers. Thematic coding will also examine how caregivers' recommendations generalize to other evidence-based digital health interventions. Among caregivers using SHUTi, we will test whether the effects of SHUTi on cognitive mechanisms of change targeted by SHUTi (i.e., more adaptive sleep beliefs, internalized sleep locus of control) are associated with differences in caregiving-related user or environment characteristics.

6. Conditions and Keywords

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

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
SHUTi (Sleep Healthy Using the Internet)
Arm Type
Experimental
Arm Description
Participants will be assigned to the SHUTi (Sleep Healthy Using the Internet) online intervention. They will spend 1-2 hours each week for 6-9 weeks completing daily sleep diaries as well as interactive core content covering topics of sleep behaviors, sleep thoughts, sleep education, and relapse prevention. As users progress through the intervention, they will receive automated, tailored instructions for how to improve their sleep.
Intervention Type
Behavioral
Intervention Name(s)
SHUTi (Sleep Healthy Using the Internet)
Other Intervention Name(s)
Cognitive-behavioral therapy for insomnia, CBT-I
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 engagement
Description
Level of SHUTi engagement: Core completion (i.e., nonuser [no cores completed], incomplete user [1-3 Cores], or complete user [4-6 Cores])
Time Frame
9-week Post-assessment
Secondary Outcome Measure Information:
Title
Open-ended feedback on SHUTi
Description
Non-users' post-assessment will include an open-ended survey regarding barriers to SHUTi adoption, the extent to which barriers were related to caregiving, and what modifications may have increased their motivation to try SHUTi. Users' (i.e., incomplete and complete) post-assessment will include an open-ended survey assessing SHUTi usage barriers and motivations, the extent to which these were related to caregiving, and how tailoring may improve usage by increasing salience to caregivers.
Time Frame
9-week Post-assessment
Title
SHUTi evaluation
Description
Items from the Internet Intervention Utility, Evaluation, and Adherence questionnaire assess users' perceived usability, acceptability, and perceived efficacy of SHUTi as well as barriers to program use
Time Frame
9-week Post-assessment
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 Pre-assessment and 9-week Post-assessment
Title
Sleep self-efficacy
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 Pre-assessment and 9-week Post-assessment
Other Pre-specified Outcome Measures:
Title
Caregiving strain
Description
Pearlin Stress Scale - Overload subscale; 4 items; averaged scores range from 1 to 4 (higher scores indicate greater perceived burden)
Time Frame
Baseline Pre-assessment and 9-week Post-assessment
Title
Insomnia symptom severity
Description
Insomnia severity index; 2 items; summed scores range from 0 to 8 (higher scores indicate more severe insomnia symptoms)
Time Frame
Baseline Pre-assessment and 9-week Post-assessment
Title
Sleep onset latency (SOL)
Description
Data collected from sleep diary: Time fell asleep - Time attempting to fall asleep
Time Frame
Baseline Pre-assessment and 9-week Post-assessment
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 Pre-assessment and 9-week Post-assessment
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 Pre-assessment and 9-week Post-assessment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Self-report providing high-intensity unpaid care (e.g., practical, medical, and/or emotional support) to a family member or "family-like" close individual, operationalized as a function of time spent caregiving and care task involvement. Self-report expecting to continue provide high-intensity care for at least another 3 months. Have access to any Internet-enabled device (computer, tablet, smartphone) and willing to be emailed about the study. Insomnia severity index score >= 10 Residing in the United States or U.S. territory English literacy Exclusion Criteria: Unusual average bed/wake times, including for shift work Current behavioral/psych treatment for insomnia Medical contraindication (Restless Leg Syndrome/Periodic Limb Movement Disorder, Obstructive Sleep Apnea, narcolepsy, parasomnia, dementia, Parkinson's, Huntington's, stroke, traumatic brain injury, brain infection/tumor, pregnancy/breastfeeding, hyperthyroidism, cancer, severe respiratory disease, epilepsy) Psychiatric contraindications (mania/hypomania, alcohol or substance abuse/dependence) Changes to prescription medications in the past 3 months (sleep, steroid, amphetamine, other wake-promoting) Severe computer literacy challenges
Facility Information:
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15260
Country
United States
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22903
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35019846
Citation
Shaffer KM, Ritterband LM, You W, Buysse DJ, Mattos MK, Camacho F, Glazer JV, Klinger J, Donovan H. Single-Group Trial of an Internet-Delivered Insomnia Intervention Among Higher-Intensity Family Caregivers: Rationale and Protocol for a Mixed Methods Study. JMIR Res Protoc. 2022 Jan 12;11(1):e34792. doi: 10.2196/34792.
Results Reference
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Optimizing Efficiency and Impact of Digital Health Interventions for Caregivers

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