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Effectiveness of Mindfulness After a Stroke

Primary Purpose

Stroke, Caregiver Burnout

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Langerian mindfulness
Sponsored by
University of Southern California
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring mindfulness, rehabilitation, caregiver, attention to variability

Eligibility Criteria

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

Inclusion Criteria:

  • Stroke survivor or caregiver of someone who have had a stroke
  • Fluent in English
  • Have access to Internet using a computer, a tablet and/or a smart phone.

Exclusion Criteria:

  • Severe language impairments
  • Participation in regular meditation or a mindfulness program in past 3 months

Sites / Locations

  • University of Southern CaliforniaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

No Intervention

Experimental

No Intervention

Arm Label

Stroke survivors - Mindfulness intervention

Stroke survivors - Waitlist control

Caregivers - Mindfulness intervention

Caregivers - Waitlist control

Arm Description

Participants who have had a stroke who are receiving the mindfulness intervention immediately after enrollment (no wait period).

Participants who have had a stroke who are assigned to the waitlist.

Participants caring for someone who have had a stroke and receiving the mindfulness intervention immediately after enrollment (no wait period).

Participants caring for someone who have had a stroke assigned to the waitlist.

Outcomes

Primary Outcome Measures

Change from baseline on the Hospital Anxiety and Depression Scale (HADS)
The HADS assesses depression and anxiety. It is a 14-item scale with 7 items each for anxiety and depression subscales. Each item is scored from 0 to 3, with higher scores indicating higher anxiety or depressive symptoms.
Change from baseline on NIH Toolbox Perceived Stress Survey (PSS)
The PSS assesses perceived stress. It includes 10 items about the occurrence of life stressors scored from 0 (never) to 4 (very often). Higher scores indicate higher perceived stress.
Change from baseline on Single-item Sleep Quality Scale (SQS)
The SQS assesses sleep quality and includes an 11-point visual analogue scale about sleep quality in the past week (0: poor, 10: excellent sleep quality).

Secondary Outcome Measures

Change from baseline on Stroke-specific Quality of Life (SS-QOL)
The SS-QOL assesses health-related quality of life for stroke survivors. It contains 49 items in 12 domains. Items are rated on a 5-point Likert scale from 1 to 5, with higher scores indicating better functioning.
Change from baseline on World Health Organization Quality of Life-BREF (WHOQOL-BREF)
The WHOQOL assesses health-related quality of life and is used in this study to assess caregivers. It comprises 26 questions from 4 domains about health and well-being. The scores are normalized, and higher scores indicate better perceived health and well-being.
Change from baseline on Zarit Burden Interview
The Zarit Burden Interview includes 22 questions about caregiver burden rated from 0 (never) to 4 (nearly always). Higher scores indicate higher perceived burden.
change in the modified Ashworth Scale (elbow)
Measure of spasticity in the flexor and extensor muscles of the elbow. The scores range from 0 to 4, with higher scores indicating more spasticity.

Full Information

First Posted
August 19, 2021
Last Updated
October 31, 2022
Sponsor
University of Southern California
Collaborators
Harvard University, Chapman University
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1. Study Identification

Unique Protocol Identification Number
NCT05029193
Brief Title
Effectiveness of Mindfulness After a Stroke
Official Title
Effectiveness of an Online Mindfulness Program for Stroke Survivors and Their Caregivers
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 13, 2021 (Actual)
Primary Completion Date
November 30, 2023 (Anticipated)
Study Completion Date
December 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
Collaborators
Harvard University, Chapman University

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
Mindfulness is promising for individuals with neurological disorders and caregivers to improve psychological well-being. This study aims to determine the extent to which a 3-week online mindfulness intervention will improve quality of life and psychological well-being for chronic stroke survivors and their caregivers, compared to a waitlist control.
Detailed Description
Background: The incidence of depression and anxiety is much higher in stroke survivors and their caregivers compared to age-matched peers. Previous work suggests that mindfulness delivered in an online format is promising for both individuals with neurological disorders and caregivers to improve quality of life and psychological well-being. Aim: This project aims to determine the extent to which a 3-week online mindfulness intervention will improve quality of life and psychological well-being for chronic stroke survivors and their caregivers, compared to a waitlist control. The primary hypothesis is that participants in the mindfulness group will demonstrate greater improvement in quality of life and psychological well-being post-intervention compared to waitlist control participants. The secondary hypothesis is that these improvements will persist for at least 1-month post-intervention. Methods: This project uses a pragmatic, randomized, waitlist-control trial design with blinded outcome assessment. Participants (stroke survivors and caregivers) are assigned to a 3-week online mindfulness intervention, or a 2-month delayed waitlist. A battery of self-reported outcome measures and clinical tests are administered pre-intervention, post-intervention and at 1-month follow-up. Participants in the waitlist control group are also assessed at enrollment. A sample of 44 stroke survivors and 44 caregivers is targeted. Changes will be measured using a repeated analysis of variance. Conclusion: The study constitutes the initial step to understand the role of mindfulness exercises delivered remotely and the potential benefit of the intervention for stroke survivors across a wide range of disability level and their caregivers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Caregiver Burnout
Keywords
mindfulness, rehabilitation, caregiver, attention to variability

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Participants will be randomly assigned to a mindfulness intervention or a waitlist control. Participants in the waitlist control group will receive the intervention after a 2-month waiting period.
Masking
Outcomes Assessor
Masking Description
All outcome measures are self-reported measures administered via online surveys, except for one. The person performing the data analysis will be blinded to group allocation.
Allocation
Randomized
Enrollment
44 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Stroke survivors - Mindfulness intervention
Arm Type
Experimental
Arm Description
Participants who have had a stroke who are receiving the mindfulness intervention immediately after enrollment (no wait period).
Arm Title
Stroke survivors - Waitlist control
Arm Type
No Intervention
Arm Description
Participants who have had a stroke who are assigned to the waitlist.
Arm Title
Caregivers - Mindfulness intervention
Arm Type
Experimental
Arm Description
Participants caring for someone who have had a stroke and receiving the mindfulness intervention immediately after enrollment (no wait period).
Arm Title
Caregivers - Waitlist control
Arm Type
No Intervention
Arm Description
Participants caring for someone who have had a stroke assigned to the waitlist.
Intervention Type
Behavioral
Intervention Name(s)
Langerian mindfulness
Intervention Description
A 3-week Langerian mindfulness intervention will be offered entirely online. The purpose of the intervention is: 1) to increase participants' mindfulness, and 2) to encourage participants to change their beliefs about the disability associated with stroke to improve their psychological state. Mindfulness refers to the act of being aware: aware of thoughts, aware of emotions, aware of physical sensations, aware of others. The intervention consists of educational texts, daily exercises, audio recordings and videos. Five different topics related to mindfulness will be introduced throughout the intervention.
Primary Outcome Measure Information:
Title
Change from baseline on the Hospital Anxiety and Depression Scale (HADS)
Description
The HADS assesses depression and anxiety. It is a 14-item scale with 7 items each for anxiety and depression subscales. Each item is scored from 0 to 3, with higher scores indicating higher anxiety or depressive symptoms.
Time Frame
2 months
Title
Change from baseline on NIH Toolbox Perceived Stress Survey (PSS)
Description
The PSS assesses perceived stress. It includes 10 items about the occurrence of life stressors scored from 0 (never) to 4 (very often). Higher scores indicate higher perceived stress.
Time Frame
2 months
Title
Change from baseline on Single-item Sleep Quality Scale (SQS)
Description
The SQS assesses sleep quality and includes an 11-point visual analogue scale about sleep quality in the past week (0: poor, 10: excellent sleep quality).
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Change from baseline on Stroke-specific Quality of Life (SS-QOL)
Description
The SS-QOL assesses health-related quality of life for stroke survivors. It contains 49 items in 12 domains. Items are rated on a 5-point Likert scale from 1 to 5, with higher scores indicating better functioning.
Time Frame
2 months
Title
Change from baseline on World Health Organization Quality of Life-BREF (WHOQOL-BREF)
Description
The WHOQOL assesses health-related quality of life and is used in this study to assess caregivers. It comprises 26 questions from 4 domains about health and well-being. The scores are normalized, and higher scores indicate better perceived health and well-being.
Time Frame
2 months
Title
Change from baseline on Zarit Burden Interview
Description
The Zarit Burden Interview includes 22 questions about caregiver burden rated from 0 (never) to 4 (nearly always). Higher scores indicate higher perceived burden.
Time Frame
2 months
Title
change in the modified Ashworth Scale (elbow)
Description
Measure of spasticity in the flexor and extensor muscles of the elbow. The scores range from 0 to 4, with higher scores indicating more spasticity.
Time Frame
2 months

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Participants will not be excluded based on gender.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Stroke survivor or caregiver of someone who have had a stroke Fluent in English Have access to Internet using a computer, a tablet and/or a smart phone. Exclusion Criteria: Severe language impairments Participation in regular meditation or a mindfulness program in past 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marika Demers, PhD
Phone
13234421196
Email
demers@pt.usc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carolee Winstein, PhD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90089
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marika Demers, PhD
Phone
323-442-1196
Email
demers@pt.usc.edu
First Name & Middle Initial & Last Name & Degree
Carolee Winstein, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We plan to study protocol, statistical analysis plan and informed consent form on clinicaltrials.gov.
IPD Sharing Time Frame
The documents will be uploaded by October 2021.

Learn more about this trial

Effectiveness of Mindfulness After a Stroke

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