The effects of a subjective sleep improvement program on convalescent stroke patients with insomnia during hospitalization: a randomized controlled trial
Not Applicable
- Conditions
- stroke
- Registration Number
- JPRN-UMIN000041541
- Lead Sponsor
- Toyohashi Sozo University
- Brief Summary
Following the intervention, the OSA-MA sleep inventory score was significantly higher in the intervention group than in the control group for factor 1, sleepiness on rising (p = .010), factor 4, refreshing (p = .004) and factor 5, sleep length (p = .001).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 82
Inclusion Criteria
Not provided
Exclusion Criteria
Those who have serious complications or physical symptoms that cannot implement the program contents Sleep disorders other than insomnia Those who have no sleep above the cutoff value using the Athens Insomnia Scale Those who take regular sleeping pills Person with dementia Those with a diagnosis of depression or mental illness Persons with physical disorders accompanied by sleep disorders Stroke patients undergoing medical treatment in a private room
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The MA version of the OSA Sleep Questionnaire calculates the average pre- and post-program 7-day scores for the five subscales, and the amount of pre- and post-program change for each subscale
- Secondary Outcome Measures
Name Time Method