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Psychosocial Wellbeing Following Stroke

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Marit Kirkevold, University of Oslo
ClinicalTrials.gov Identifier:
NCT01912014
First received: July 24, 2013
Last updated: July 29, 2013
Last verified: July 2013

July 24, 2013
July 29, 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 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01912014 on ClinicalTrials.gov Archive Site
Change from baseline in Stroke and Aphasia Quality of Life (SAQOL-39) [ Time Frame: baseline and 12 months after end of intervention ] [ Designated as safety issue: No ]
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
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Norway
 
NCT01912014
2.2007.37 (REK), 16369 (Social science data)
Yes
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