Psychosocial Wellbeing Following Stroke

Phase 2CompletedNCT01912014

University of Oslo25 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Enrollment

Conditions

Psychosocial Narrative Coping Quality of Life

Interventions

Psychosocial support and counsellingBEHAVIORAL

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Oslo University hospital

Oslo, Oslo, Norway

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)

Time frame: baseline and 12 months after end of intervention

Data from ClinicalTrials.gov

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