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Psychosocial Wellbeing Following Stroke

U

University of Oslo

Status and phase

Completed
Phase 2
Phase 1

Conditions

Narrative
Coping
Quality of Life
Psychosocial

Treatments

Behavioral: Psychosocial support and counselling

Study type

Interventional

Funder types

Other

Identifiers

NCT01912014
2.2007.37 (REK)
16369 (Social science data)

Details and patient eligibility

About

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.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • 18 years old or above
  • acute stroke
  • 4-8 weeks poststroke

Exclusion Criteria

  • Other serious disease

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Psychosocial support and counselling
Experimental group
Description:
There is only one arm as this is a pilot and feasibility study.
Treatment:
Behavioral: Psychosocial support and counselling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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