Screening Study for the Department of Rehabilitation Medicine
Primary Purpose
Convalescence, Healthy
Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by

About this trial
This is an observational trial for Convalescence focused on measuring Rehabilitation, Functional Level, Activity of Daily Living, Mobility, Normal Volunteer
Eligibility Criteria
INCLUSION CRITERIA: In- and outpatients referred to the Rehabilitation Medicine Department. Normal volunteers of either sex.
Sites / Locations
- National Institutes of Health Clinical Center, 9000 Rockville Pike
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00023088
First Posted
August 22, 2001
Last Updated
June 30, 2017
Sponsor
National Institutes of Health Clinical Center (CC)
1. Study Identification
Unique Protocol Identification Number
NCT00023088
Brief Title
Screening Study for the Department of Rehabilitation Medicine
Official Title
Rehabilitation Medicine Screening Protocol
Study Type
Observational
2. Study Status
Record Verification Date
July 9, 2008
Overall Recruitment Status
Completed
Study Start Date
April 13, 1994 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 9, 2008 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
National Institutes of Health Clinical Center (CC)
4. Oversight
5. Study Description
Brief Summary
The primary function of the Department of Rehabilitation Medicine (RMD) is to diagnose and treat patients at the NIH who have problems in locomotion, activities of daily living, occupational roles, communication, swallowing, or problems with chronic pain. The major goal of this department s to help patients achieve maximal function so that they can resume their daily living activities as normal as possible.
In order for the department to accomplish it's goal it requires the involvement of medical staff and the use of a variety of tests and instruments. Before a new test, evaluation technique, or piece of physical equipment can be considered for use in the treatment of patients it must be carefully studied.
Researchers must make sure the test, technique, or instrument is safe, sensitive, accurate, specific, and reproducible. Therefore all of these tests, techniques, and instruments must first undergo a trial period. Normal volunteers and patients from the RMD and outside of the RMD may be selected to participate in the trial period.
This study provides a framework for researchers in the Department of Rehabilitation Medicine (RMD) to develop new tests, techniques, technology, and equipment.
Detailed Description
This protocol provides a framework for clinicians in the Department of Rehabilitation Medicine (RMD) to develop and pilot new tests, techniques, technology, or equipment to remain state-of-the-art.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Convalescence, Healthy
Keywords
Rehabilitation, Functional Level, Activity of Daily Living, Mobility, Normal Volunteer
7. Study Design
Enrollment
600 (false)
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA:
In- and outpatients referred to the Rehabilitation Medicine Department.
Normal volunteers of either sex.
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Screening Study for the Department of Rehabilitation Medicine
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