N/A
N=16
Mindfulness After Stroke
Stroke · Caregiver Burden
Bottom Line
View on ClinicalTrials.gov: NCT04553679 ↗Enrolled (actual)
16
Serious AEs
0.0%
Results posted
Feb 2023
Primary outcome: Primary: Change in Stroke Impact Scale — 2.3 score on a scale
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Mindfulness online intervention (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Southern California
- Primary completion
- Jul 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Stroke Impact Scale |
2.3 | — |
| SECONDARY Change in Hospital Anxiety and Depression Scale |
0.9; 5 | — |
| SECONDARY Change in National Institute of Health Perceived Stress Survey |
1.1; 4.5 | — |
| SECONDARY Change in Single-Item Sleep Quality Scale |
0.9; 4 | — |
| SECONDARY Change in World Health Organization Quality of Life-bref |
6.25 | — |
| SECONDARY Adapted Post-Study System Usability Questionnaire |
14.3; 24.5 | — |
| SECONDARY Change in Zarit Burden Interview |
3 | — |
Summary
The purpose of this study is to test the relevance, satisfaction and ease-of-use of an online mindfulness intervention among stroke survivors and their caregivers. Quality of life, depression, anxiety, stress and sleep quality will be assessed before, after and at 1 month after the intervention. After the intervention, participants' feedback about the usability and the satisfaction with the intervention and the online program will be gathered. Based on participants' feedback, changes to the intervention will be made to obtain a final version.
Eligibility Criteria
Inclusion Criteria
- Diagnosis of stroke (for stroke survivors) or caregiver of someone who have had a stroke
- Ability to access Internet using a computer, a tablet and/or a smart phone
- Ability to provide informed consent
- Fluent in English
Exclusion Criteria
- Severe language impairments
- Regular meditation or participation in a mindfulness program in the past 3 months
Data sourced from ClinicalTrials.gov (NCT04553679). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.