Psychosocial Wellbeing Following Stroke
Phase 1
Completed
- Conditions
- PsychosocialNarrativeCopingQuality of Life
- Registration Number
- NCT01912014
- Lead Sponsor
- University of Oslo
- Brief Summary
The purpose of this feasibility study is to develop and initially test a dialogue-based psychosocial intervention aimed at promoting coping and psychosocial wellbeing following an acute stroke. The intervention is carried out by primary care registered nurses or other appropriate health professionals. The intervention included persons with and without aphasia.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
- 18 years old or above
- acute stroke
- 4-8 weeks poststroke
Exclusion Criteria
- Other serious disease
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39) baseline and 2 weeks after end of intervention
- Secondary Outcome Measures
Name Time Method Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39) baseline and 12 months after end of intervention
Trial Locations
- Locations (1)
Oslo University hospital
🇳🇴Oslo, Norway
Oslo University hospital🇳🇴Oslo, Norway