Self-management EdUcation and SuPport to Promote PsychOsocial Health Among StRoke Survivors and Informal Caregivers in a VirTual Stroke Community (SUPPORT) (SUPPORT)
Primary Purpose
Stroke
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Learning in a Virtual Environment (LIVE)
Sponsored by

About this trial
This is an interventional other trial for Stroke focused on measuring depression, anxiety
Eligibility Criteria
Inclusion Criteria:
- Stroke survivors that have experienced an ischemic or hemorrhagic stroke event and their caregivers
- can read, write, and speak English
- are able to provide written consent
- are computer literate (have used a computer for ≥1 month)
- have access to a computer with broadband internet at home
- understand how to use the Internet (accessed the Internet on ≥2 occasions)
Exclusion Criteria:
- reside outside of the home
- Montreal Cognitive Assessment score of <9 indicating moderate to severe impairment
- Caregivers that provide long-distance care. I
Sites / Locations
- The University of Texas Health Science Center at Houston
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment
Arm Description
Outcomes
Primary Outcome Measures
Feasibility as assessed by the number of participants enrolled in the study
This will be defined as the number enrolled divided by the number of eligible individuals screened
Feasibility as assessed by the number of participants who complete the study
Feasibility as assessed by the number of participants who complete the data collection forms
Usability as assessed by the perceived usefulness score
Usability as assessed by the perceived ease of use scores
This has 10 items, each scored form 1(strongly disagree) to 5(strongly agree), higher score meaning higher perceived ease of use
Usability as assessed by the number of times the participants log in
Usability as assessed by the time spent in the environment in minutes
Acceptability as assessed by the number of VE Meetings attended
Acceptability as assessed by the number of VE objects manipulated
Objects manipulated are the resources interacted with
Secondary Outcome Measures
Change in perceived social support as assessed by the Multidimensional Scale of Perceived Social Support (MSPSS)
This is a 12 item scale , each question is scored from 1(very strongly disagree) to 7(very strongly agree) for a maximum score of score of 84, a higher number indicating more social support
Change in post stroke depression as assessed by the Patient Health Questionnaire-9 score (PHQ-9)
This is a 9 item questionnaire, each scored from 0(not at all) to 3(nearly every day), a higher number indication g more depression
Change in anxiety as assessed by the Generalized Anxiety Disorder-7 score
This is a 7 item questionnaire, each is scored from 0(not at all) to 3(nearly every day) a higher number indicating more anxiety
Change in loneliness as assessed by the UCLA loneliness scale scores
This is a 20 item questionnaire, each one is scored form 1(never) to 4(always). Scores for questions 1,5,6,9,10,15,16,19 and 20 are reversed(i.e. 1=4,2=3,3=2,4=1)and the scores for each item is then summed together, higher number indicating more loneliness
Change in caregiver burden as assessed by the Zarit Burden Interview (ZBI)
This is a 22 item questionnaire,each one scored from 0(never)-4(nearly always) higher core indicating more burden
Change in self efficacy ( ability to perform tasks or behaviors) as assessed by the PROMIS General Self-efficacy Form
This is a 10 item questionnaire, each one is scored from 1(not at all true) to 4(exactly true), a higher number indicating a better outcome
Change in emotional support as assessed by the NIH Emotional Support Form
This is an 8 item questionnaire, and each is scored form 1(never)-5(always), for a maximum score of 40, a higher number indicating higher levels of emotional support
Change in instrumental support as assessed by the PROMIS Short Form v2.0
This is an 8 item questionnaire, and each is scored form 1(never)-5(always), for a maximum score of 40, a higher number indicating higher levels of instrumental support
Change in ability to recover form stress as measured by the Brief Resilience Scale
This is a 6 item questionnaire scored from 1 (strongly disagree) to 5 (strongly agree) a higher number indicating a better outcome?
Change in the amount that pain interferes with daily life as assessed by the PROMIS Short Form Pain Interference v 1.0 8a
This is an 8 item questionnaire and each is scored from 1 (not at all) to 5 (very much) a higher number indicating a worse outcome
Full Information
NCT ID
NCT05487144
First Posted
August 2, 2022
Last Updated
January 8, 2023
Sponsor
The University of Texas Health Science Center, Houston
1. Study Identification
Unique Protocol Identification Number
NCT05487144
Brief Title
Self-management EdUcation and SuPport to Promote PsychOsocial Health Among StRoke Survivors and Informal Caregivers in a VirTual Stroke Community (SUPPORT)
Acronym
SUPPORT
Official Title
Self-management EdUcation and SuPport to Promote PsychOsocial Health Among StRoke Survivors and Informal Caregivers in a VirTual Stroke Community (SUPPORT): A Pilot Project
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
April 27, 2022 (Actual)
Primary Completion Date
November 18, 2022 (Actual)
Study Completion Date
November 18, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston
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 purpose of this study is to create a virtual stroke community for stroke survivors and informal caregivers of stroke survivors by customizing an existing VE intervention to incorporate real-time, stroke-specific, psychosocial self management education (SME) and social interactions, to test feasibility, acceptability, and usability of the customized intervention for stroke survivors and informal caregivers of stroke survivors and to obtain and explore data to derive evidence-based hypotheses and properly design and conduct a future, larger trial to demonstrate treatment efficacy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
depression, anxiety
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Learning in a Virtual Environment (LIVE)
Intervention Description
Phase 1 of the study will be a one-time meeting, either remote or in-person to complete V.E. training and fill out questionnaires. Phase 2 of the study is the 8 week intervention implementation.Participants will access the V.E. community from their homes on a computer with broadband internet. During the first four weeks of the intervention, participants will be required to come into the V.E. at least once per week for at least one hour. For the last four weeks, V.E. participation is strongly encouraged, but not required. The content in the V.E. will focus on psychosocial health and stroke recovery, and the messaging in the VE will be updated bi-weekly to encourage retention and engagement. Group meetings led by the study PI, a psychologist, or another trained member of the research team at least once a week will be offered. During the intervention period, VE-specific data will be collected continuously. Phase 3, will include a survey and a focus group interview via online platform.
Primary Outcome Measure Information:
Title
Feasibility as assessed by the number of participants enrolled in the study
Description
This will be defined as the number enrolled divided by the number of eligible individuals screened
Time Frame
post intervention (8 weeks from baseline of last participant )
Title
Feasibility as assessed by the number of participants who complete the study
Time Frame
post intervention (8 weeks from baseline of last participant )
Title
Feasibility as assessed by the number of participants who complete the data collection forms
Time Frame
post intervention (8 weeks from baseline of last participant )
Title
Usability as assessed by the perceived usefulness score
Time Frame
post intervention (8 weeks from baseline)
Title
Usability as assessed by the perceived ease of use scores
Description
This has 10 items, each scored form 1(strongly disagree) to 5(strongly agree), higher score meaning higher perceived ease of use
Time Frame
post intervention (8 weeks from baseline)
Title
Usability as assessed by the number of times the participants log in
Time Frame
post intervention (8 weeks from baseline)
Title
Usability as assessed by the time spent in the environment in minutes
Time Frame
post intervention (8 weeks from baseline)
Title
Acceptability as assessed by the number of VE Meetings attended
Time Frame
post intervention (8 weeks from baseline)
Title
Acceptability as assessed by the number of VE objects manipulated
Description
Objects manipulated are the resources interacted with
Time Frame
post intervention (8 weeks form baseline)
Secondary Outcome Measure Information:
Title
Change in perceived social support as assessed by the Multidimensional Scale of Perceived Social Support (MSPSS)
Description
This is a 12 item scale , each question is scored from 1(very strongly disagree) to 7(very strongly agree) for a maximum score of score of 84, a higher number indicating more social support
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in post stroke depression as assessed by the Patient Health Questionnaire-9 score (PHQ-9)
Description
This is a 9 item questionnaire, each scored from 0(not at all) to 3(nearly every day), a higher number indication g more depression
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in anxiety as assessed by the Generalized Anxiety Disorder-7 score
Description
This is a 7 item questionnaire, each is scored from 0(not at all) to 3(nearly every day) a higher number indicating more anxiety
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in loneliness as assessed by the UCLA loneliness scale scores
Description
This is a 20 item questionnaire, each one is scored form 1(never) to 4(always). Scores for questions 1,5,6,9,10,15,16,19 and 20 are reversed(i.e. 1=4,2=3,3=2,4=1)and the scores for each item is then summed together, higher number indicating more loneliness
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in caregiver burden as assessed by the Zarit Burden Interview (ZBI)
Description
This is a 22 item questionnaire,each one scored from 0(never)-4(nearly always) higher core indicating more burden
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in self efficacy ( ability to perform tasks or behaviors) as assessed by the PROMIS General Self-efficacy Form
Description
This is a 10 item questionnaire, each one is scored from 1(not at all true) to 4(exactly true), a higher number indicating a better outcome
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in emotional support as assessed by the NIH Emotional Support Form
Description
This is an 8 item questionnaire, and each is scored form 1(never)-5(always), for a maximum score of 40, a higher number indicating higher levels of emotional support
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in instrumental support as assessed by the PROMIS Short Form v2.0
Description
This is an 8 item questionnaire, and each is scored form 1(never)-5(always), for a maximum score of 40, a higher number indicating higher levels of instrumental support
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in ability to recover form stress as measured by the Brief Resilience Scale
Description
This is a 6 item questionnaire scored from 1 (strongly disagree) to 5 (strongly agree) a higher number indicating a better outcome?
Time Frame
Baseline, post intervention (8 weeks after baseline)
Title
Change in the amount that pain interferes with daily life as assessed by the PROMIS Short Form Pain Interference v 1.0 8a
Description
This is an 8 item questionnaire and each is scored from 1 (not at all) to 5 (very much) a higher number indicating a worse outcome
Time Frame
Baseline, post intervention (8 weeks after baseline)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Stroke survivors that have experienced an ischemic or hemorrhagic stroke event and their caregivers
can read, write, and speak English
are able to provide written consent
are computer literate (have used a computer for ≥1 month)
have access to a computer with broadband internet at home
understand how to use the Internet (accessed the Internet on ≥2 occasions)
Exclusion Criteria:
reside outside of the home
Montreal Cognitive Assessment score of <9 indicating moderate to severe impairment
Caregivers that provide long-distance care. I
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Beauchamp, PhD, RN
Organizational Affiliation
The University of Texas Health Science Center, Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Texas Health Science Center at Houston
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Self-management EdUcation and SuPport to Promote PsychOsocial Health Among StRoke Survivors and Informal Caregivers in a VirTual Stroke Community (SUPPORT)
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