Psychosocial Wellbeing Following Stroke

Phase 1

Completed

• Conditions: Psychosocial; Narrative; Coping; Quality of Life
• Interventions: Behavioral: Psychosocial support and counselling

• 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

Study Timeline

• Study Start: 2007-01
• Primary Completion: 2011-04
• Study Completion: 2011-12
• Status Verified: 2013-07
• Study First Submitted: 2013-07-24
• Study First Submitted QC: 2013-07-29
• Last Update Submitted: 2013-07-29
• Study First Posted: 2013-07-30
• Last Update Posted: 2013-07-30

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

Arm && Interventions

Group	Intervention	Description
Psychosocial support and counselling	Psychosocial support and counselling	There is only one arm as this is a pilot and feasibility study.

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