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Clinical Trials/NCT02861638
NCT02861638CompletedNot Applicable

Effects of Action Observation Therapy in Patients Recovering From Total Hip Arthroplasty: A Prospective Clinical Trial

Fondazione Don Carlo Gnocchi Onlus0 sites30 target enrollmentStarted: April 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Primary Endpoint
Change of Pain intensity

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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);

Arms & Interventions

Experimental group

Experimental

Video of the exercises and conventional physiotherapy. 30 minutes twice a day, 5 days a week for 2 weeks.

Intervention: Experimental group (Device)

Experimental group

Experimental

Video of the exercises and conventional physiotherapy. 30 minutes twice a day, 5 days a week for 2 weeks.

Intervention: Conventional physiotherapy (Device)

Control group

Active Comparator

Video of nature scenes and conventional physiotherapy. 30 minutes twice a day, 5 days a week for 2 weeks.

Intervention: Control group (Device)

Control group

Active Comparator

Video of nature scenes and conventional physiotherapy. 30 minutes twice a day, 5 days a week for 2 weeks.

Intervention: Conventional physiotherapy (Device)

Outcomes

Primary Outcomes

Change of Pain intensity

Time Frame: Baseline and immediately post-intervention

Visual Analogue Scale (VAS)

Change of Range Of Motion (ROM)

Time Frame: Baseline and immediately post-intervention

Active and passive range of motion of hip

Secondary Outcomes

  • Barthel index(Baseline and immediately post-intervention)
  • Short Form-36 motor(Baseline and immediately post-intervention)
  • Tinetti scale(Baseline and immediately post-intervention)
  • Lequesne index(Baseline and immediately post-intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jorge Hugo Villafañe, PhD

Researcher

Fondazione Don Carlo Gnocchi Onlus

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