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Survey on Return to Work After Stroke

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01699035
First Posted: October 3, 2012
Last Update Posted: September 12, 2014
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.
Collaborator:
U.S. Department of Education
Information provided by (Responsible Party):
Robert Hartke, Rehabilitation Institute of Chicago
  Purpose
Survey of survivor perspective on critical elements that either facilitate or inhibit return to work after a stroke. Critical elements are queried in areas of finances, stroke impairments, interpersonal support, therapeutic support, organization influences, work or job specific issues and psychological issues.

Condition
Stroke

Study Type: Observational
Study Design: Time Perspective: Cross-Sectional
Official Title: Survivor Perspective on Critical Factors to Return to Work After Stroke

Further study details as provided by Robert Hartke, Rehabilitation Institute of Chicago:

Primary Outcome Measures:
  • critical factors that facilitate or inhibit return to work after stroke [ Time Frame: after collection of data on all surveys ]
    38 multiple choice items that assess psychological factors important to return to work, financial incentives and disincentives, the role of stroke impairments, interpersonal supports that facilitate and inhibit return, the role of therapeutic support especially vocational rehabilitation, organizational influences, and work specific issues that impact on return. Demographic information is also queried including work type and current work status. Data will be analyzed descriptively by these critical factors and also by other demographic factors such as age, work status, and race.


Enrollment: 715
Study Start Date: February 2012
Study Completion Date: September 2014
Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
stroke survivors
stroke survivors who have either returned to work, have thought about returning to work, or have tried to return to work

Detailed Description:
The objective of this project is to more accurately describe the stroke survivor's perspective on return to work. The survey development included qualitative analysis of a set of interviews with stroke survivors to arrive at the critical elements described above, followed by item development with an expert panel and preliminary testing of the wording and format for legibility. The survey is being administered both on-line and by paper through the mail to a wide range of survivors with the objective of obtaining a large, diverse sample. The ultimate goal of the project is to arrive at a refined set of recommendations to inform stroke survivors, health care professionals and employers to increase their sensitivity to the needs and desires of individual attempting to return to work after stroke.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
stroke survivors
Criteria

Inclusion Criteria:

  • have returned to work, have thought about returning to work, or have tried to return to work

Exclusion Criteria:

  • non-stroke disability
  • retired or no plan to return to work
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01699035


Locations
United States, Illinois
Rehabilitation Institute of Chicago
Chicago, Illinois, United States, 60611
Sponsors and Collaborators
Shirley Ryan AbilityLab
U.S. Department of Education
Investigators
Principal Investigator: Robert J Hartke, Ph.D. Shirley Ryan AbilityLab
  More Information

Publications:
Responsible Party: Robert Hartke, Lead Psychologist, Rehabilitation Institute of Chicago
ClinicalTrials.gov Identifier: NCT01699035     History of Changes
Other Study ID Numbers: H133B080031
First Submitted: October 1, 2012
First Posted: October 3, 2012
Last Update Posted: September 12, 2014
Last Verified: September 2014

Keywords provided by Robert Hartke, Rehabilitation Institute of Chicago:
stroke
work
vocational rehabilitation

Additional relevant MeSH terms:
Stroke
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases