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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03659409
Other study ID # 2016/2361
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 12, 2016
Est. completion date December 31, 2018

Study information

Verified date March 2020
Source Singapore General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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).


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.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 80 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.
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.

Locations

Country Name City State
Singapore Singapore General Hospital Singapore

Sponsors (1)

Lead Sponsor Collaborator
Singapore General Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Other Mental Fatigue Scale (MFS) A 15-item questionnaire that cover the most common symptoms that occur after brain injury such as that sustained after a stroke. 1 Month
Primary Cohen Perceived Stress Scale A 10-item measure evaluating the perception of stress. Past 1 Month
Primary Centre for Epidemiologic Studies Depression Scale (CES-D) A 20-item measure for epidemiological research on depression. Past 1 Week
Primary Stroke Specific Quality of Life Scale (SS-QOL) A 49-item self-report questionnaire designed to measure the heath related quality of life specific to stroke survivors across 12 domains. Past 1 Month
Primary Stroke Impact Scale (SIS) A 64-item questionnaire that assesses across 8 domains 1 week
Primary Short-Form-36 (SF-36) A 36-item self-report survey of health, including physical and mental health. Higher scaled scores reflect better quality of health. A range from the past 4 to 52 weeks
Secondary Zarit Burden Interview A 22-item self-report questionnaire to measure for level of caregiver burden or stress. Past 1 Month
Secondary Five Facet Mindfulness Questionnaire 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. Past 1 Month
Secondary Big Five Personality Inventory 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. Past 1 Month
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