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Psychosocial Wellbeing Following Stroke

Phase 1
Completed
Conditions
Psychosocial
Narrative
Coping
Quality 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
NameTimeMethod
Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39)baseline and 2 weeks after end of intervention
Secondary Outcome Measures
NameTimeMethod
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

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