SOM: Stroke Of Mindfulness: Investigating Physiological and Psychological Well-being
Study Details
Study Description
Brief Summary
This study evaluates the impact of mindfulness-based interventions on psycho-social and physiological well-being among stroke survivors and their family caregivers. This study will employ a treatment wait-list cross-over design, with half the participants randomized to receive the intervention first (treatment group), while the other half receives the interventions 2 months following the end of the treatment phase (wait-list group).
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Stroke survivors face many concerns, including the physical, psychological, cognitive and psychosocial consequences of stroke, as well as impaired function and quality of life. Also important for stroke survivors is the possibility of recurrence that may result in death and further disability. Survivors depend on their caregivers to provide assistance for daily living tasks, emotional support and taking on new roles and responsibilities with changing social dynamics, often causing long-term strain.
Mindfulness-based interventions (MBIs) are psychotherapeutic interventions which have been shown to improve psychological, physiological and psychosocial outcomes such as anxiety, depression, mental fatigue, blood pressure and overall quality of life. However, data is limited for stroke survivors and their caregivers, especially in Asians. This study will evaluate the impact of MBIs on the psychological well-being and perceived quality of life among stroke survivors and their family caregivers in Singapore.
This study employs a randomized treatment-waitlist crossover design with outcome measures administered before and after the intervention as well as at 3 months follow-up for the treatment group.
The intervention consists of 4 weekly 2-hour mindfulness sessions. Participants will be introduced, taught and guided in practice of mindfulness-based interventions that are focused on their (1) breath, (2) senses, (3) body and bodily movement, (4) feelings of empathy and compassion. Pre- and post-intervention questionnaires will be conducted to assess symptoms associated with depression, anxiety, stress and perceived quality of life. Blood pressure and heart rate variability recordings before and after intervention will also be noted.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Mindfulness Based Intervention 4 weekly 2-hour sessions. Participants will be introduced, taught and guided in practice of mindfulness-based interventions that are focused on their (1) breath, (2) senses, (3) body and bodily movements, (4) feelings of empathy and compassion. |
Behavioral: Mindfulness-Based Intervention
4 weekly 2-hour sessions. Participants will be introduced, taught and guided in practice of mindfulness-based interventions that are focused on their (1) breath, (2) senses, (3) body and bodily movements, (4) feelings of empathy and compassion.
|
| Other: Treatment Waitlist Group Participants will receive no intervention, except for a baseline follow-up at the start and again at the end of the first phase. 2 months after the end of the first intervention phase, participants in this group will receive the same mindfulness-based intervention for 4 weeks. |
Behavioral: Waitlist - Mindfulness-Based Intervention
Participants in this group will only receive the Mindfulness-Based Intervention 3-months after they have started the study and baseline measurements. While participants in the Intervention Arm are receiving the treatment, this group will receive No intervention for the first four weeks and will continue as treatment as usual until it is their turn to receive the Intervention.
|
Outcome Measures
Primary Outcome Measures
- Cohen Perceived Stress Scale [Past 1 Month]
A 10-item measure evaluating the perception of stress.
- Centre for Epidemiologic Studies Depression Scale (CES-D) [Past 1 Week]
A 20-item measure for epidemiological research on depression.
- Stroke Specific Quality of Life Scale (SS-QOL) [Past 1 Month]
A 49-item self-report questionnaire designed to measure the heath related quality of life specific to stroke survivors across 12 domains.
- Stroke Impact Scale (SIS) [1 week]
A 64-item questionnaire that assesses across 8 domains
- Short-Form-36 (SF-36) [A range from the past 4 to 52 weeks]
A 36-item self-report survey of health, including physical and mental health. Higher scaled scores reflect better quality of health.
Secondary Outcome Measures
- Zarit Burden Interview [Past 1 Month]
A 22-item self-report questionnaire to measure for level of caregiver burden or stress.
- Five Facet Mindfulness Questionnaire [Past 1 Month]
This 39-item instrument is based on a factor analytic study of five independently developed mindfulness questionnaires. The analysis yielded five factors that appear to represent elements of mindfulness as it is currently conceptualized. The five facets are observing, describing, acting with awareness, non-judging of inner experience, and non-reactivity to inner experience.
- Big Five Personality Inventory [Past 1 Month]
44-item inventory that measures an individual on the Big Five Factors (dimensions) of personality (Goldberg, 1993). Each of the factors is then further divided into personality facets.
Other Outcome Measures
- Mental Fatigue Scale (MFS) [1 Month]
A 15-item questionnaire that cover the most common symptoms that occur after brain injury such as that sustained after a stroke.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Stroke Survivors
-
Family Caregivers
-
Able to speak and understand English Fluently
-
Comprehends and provides consent independently
Exclusion Criteria:
-
Cognitively impaired individuals with a MMSE Score of less than 20, MoCA score of less than 23
-
Depression and Anxiety Stress Scale Scores, DASS, Depression >7, Anxiety >8, and Stress >13
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Singapore General Hospital | Singapore | Singapore | 169608 |
Sponsors and Collaborators
- Singapore General Hospital
Investigators
- Principal Investigator: Kinjal Doshi, PhD, Singapore General Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2016/2361