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OpenTrials
Completed

NCT Number: NCT01912014

Psychosocial Wellbeing Following Stroke

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Oslo University hospital

Oslo, Norway

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Other serious disease

Treatment and study plan

Psychosocial support and counselling

Behavioral

Primary outcomes

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

    Time frame: baseline and 2 weeks after end of intervention

Secondary outcomes

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

    Time frame: baseline and 12 months after end of intervention

Sponsors and collaborators

Lead sponsor

University of Oslo

Other

Registry information

Official study title

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

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Jul 30, 2013
Registry last updated
Jul 30, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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