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Psychosocial Wellbeing Following Stroke

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01912014
First Posted: July 30, 2013
Last Update Posted: July 30, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Marit Kirkevold, University of Oslo
July 24, 2013
July 30, 2013
July 30, 2013
January 2007
April 2011   (Final data collection date for primary outcome measure)
Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39) [ Time Frame: baseline and 2 weeks after end of intervention ]
Same as current
No Changes Posted
Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39) [ Time Frame: baseline and 12 months after end of intervention ]
Same as current
Not Provided
Not Provided
 
Psychosocial Wellbeing Following Stroke
Psychosocial Wellbeing Following Stroke: Developing and Testing a Psychosocial Nursing Intervention for Primary Care
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.
Not Provided
Interventional
Phase 1
Phase 2
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
  • Psychosocial
  • Narrative
  • Coping
  • Quality of Life
Behavioral: Psychosocial support and counselling
Experimental: Psychosocial support and counselling
There is only one arm as this is a pilot and feasibility study.
Intervention: Behavioral: Psychosocial support and counselling

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
25
December 2011
April 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

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

Exclusion Criteria

  • Other serious disease
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Norway
 
 
NCT01912014
2.2007.37 (REK)
16369 (Social science data)
Yes
Not Provided
Not Provided
Marit Kirkevold, University of Oslo
University of Oslo
Not Provided
Not Provided
University of Oslo
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP