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Clinical Trials/NCT01912014
NCT01912014
Completed
Phase 1

Psychosocial Wellbeing Following Stroke: Developing and Testing a Psychosocial Nursing Intervention for Primary Care

University of Oslo1 site in 1 country25 target enrollmentJanuary 2007
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ConditionsPsychosocialNarrativeCopingQuality of Life

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Psychosocial
Sponsor
University of Oslo
Enrollment
25
Locations
1
Primary Endpoint
Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39)
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2011
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marit Kirkevold

Professor

University of Oslo

Eligibility Criteria

Inclusion Criteria

  • •18 years old or above
  • •acute stroke
  • •4-8 weeks poststroke
  • •Exclusion Criteria
  • •Other serious disease

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39)

Time Frame: baseline and 2 weeks after end of intervention

Secondary Outcomes

  • Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39)(baseline and 12 months after end of intervention)

Study Sites (1)

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