- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02435134
Examination Chair for Hip Internal Rotation Range of Motion Measurement (HIRROM)
February 13, 2017 updated by: Schulthess Klinik
Validation of a Test Protocol for Measuring the Hip Internal Rotation Range of Motion Using a Newly Developed Examination Chair
Hip internal rotation range of motion (HIRROM) assessment is performed to assess the mobility of the hip.
The assessment is typically done manually (manual testing), which induces large variability in the results between and within testers.
An initial version of an examination chair (EC1) was recently developed with the aim to minimize the variability of testing results for HIRROM assessments.
A new version of the examination chair (EC2) has been implemented in order to individualize the testing protocol and will be validated in this study.
Study Overview
Study Type
Observational
Enrollment (Actual)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Zurich, Switzerland, 8008
- Schulthess Klinik
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthy participants
Description
Inclusion Criteria:
- Participants are pain free in the lower extremity, hip and back
- Participants signed the consent form
Exclusion Criteria:
- Participant requires pain relief medication
- History of hip surgery
- Neuromuscular disorders
- Legal incompetence
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Healthy participants
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hip internal rotation range of motion angle (degrees)
Time Frame: 7 days
|
Participants will be tested for hip internal range of motion using three different methods.
The measurements will be repeated 7 days after the initial measurement.
|
7 days
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 7, 2015
Primary Completion (Actual)
January 25, 2017
Study Completion (Actual)
January 25, 2017
Study Registration Dates
First Submitted
April 27, 2015
First Submitted That Met QC Criteria
May 5, 2015
First Posted (Estimate)
May 6, 2015
Study Record Updates
Last Update Posted (Actual)
February 14, 2017
Last Update Submitted That Met QC Criteria
February 13, 2017
Last Verified
February 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- HIRROM
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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