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Personality Type as a Predictor to Develop Depression and Reduction in Quality of Life Among Stroke Survivals. (TPQ BDI SSQOL)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00845455
First Posted: February 18, 2009
Last Update Posted: October 25, 2011
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):
d_yarnitsky, Rambam Health Care Campus
  Purpose
Personality type as a predictor to develop depression and reduction in quality of life among stroke survivals.

Condition
Stroke Depression Quality of Life Personality Type

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Personality Type as a Predictor to Develop Depression and Reduction in Quality of Life Among Stroke Survivals.

Further study details as provided by d_yarnitsky, Rambam Health Care Campus:

Primary Outcome Measures:
  • Depression [ Time Frame: 1-3 month post stroke ]

Secondary Outcome Measures:
  • QOL post stroke [ Time Frame: 1-3 month post stroke ]

Enrollment: 85
Study Start Date: November 2007
Study Completion Date: June 2009
Primary Completion Date: June 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
1. Harm Avoidance
Personality type
2. Reward Dependence
Personality type
3. Novelty Seeking
Personality type

  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:   40 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Stroke ( TIA, CVA, ICH ) patients
Criteria

Inclusion Criteria:

  • any stroke,
  • age 40-90,
  • able to sigh informed concent,
  • able to fill in the questionnaires.

Exclusion Criteria:

  • non stroke,
  • previous depression,
  • not able to give consent or answer the questions.
  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): NCT00845455


Sponsors and Collaborators
d_yarnitsky
Investigators
Principal Investigator: David - Yarnitsky, Prof.
  More Information

Responsible Party: d_yarnitsky, MD, Rambam Health Care Campus
ClinicalTrials.gov Identifier: NCT00845455     History of Changes
Other Study ID Numbers: TPQStroke03CTIL
First Submitted: February 15, 2009
First Posted: February 18, 2009
Last Update Posted: October 25, 2011
Last Verified: October 2011

Additional relevant MeSH terms:
Stroke
Depression
Depressive Disorder
Personality Disorders
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases
Behavioral Symptoms
Mood Disorders
Mental Disorders