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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02861638
Other study ID # Hip Replacement
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2014
Est. completion date October 2014

Study information

Verified date August 2020
Source Fondazione Don Carlo Gnocchi Onlus
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Postoperative rehabilitation is required for a successful outcome following total hip arthroplasty. Traditionally rehabilitative programs aim to increase range of motion, to strengthen quadriceps, to restore normal gait, and to recover independence in activities of daily living. In the last decade action observation treatment, in addition to conventional physiotherapy has been proposed as a treatment method in rehabilitative medicine. There is growing evidence of the applicability of action observation training in rehabilitative medicine, indeed it has been applied in the rehabilitation of stroke of Parkinson disease of cerebral palsy and of aphasia.

Nevertheless those are small studies and one of them included a mixed population of hip and knee arthroplasty.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 2014
Est. primary completion date September 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Primary total hip replacement.

Exclusion Criteria:

- bilateral hip replacement

- previous total hip replacement.

- pre-existing motor impairment (i.e. hemiparesis, poliomyelitis, lumbar sciatica);

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Experimental group
Video of the exercises
Control group
video of nature scenes
Conventional physiotherapy
Mobilization, exercises and transfer practice.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Don Carlo Gnocchi Onlus

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Pain intensity Visual Analogue Scale (VAS) Baseline and immediately post-intervention
Primary Change of Range Of Motion (ROM) Active and passive range of motion of hip Baseline and immediately post-intervention
Secondary Barthel index Barthel Index of Activities of Daily Living Baseline and immediately post-intervention
Secondary Short Form-36 motor The Medical Outcome Study 36-Item Short Form Health Survey (SF-36) is a widely used method to evaluate health-related quality of life Baseline and immediately post-intervention
Secondary Tinetti scale Balance Baseline and immediately post-intervention
Secondary Lequesne index The Lequesne Index is a 10-question survey given to patients with osteoarthritis of the knee Baseline and immediately post-intervention
See also
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