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Action Observation in Hip Replacement

D

Don Carlo Gnocchi Onlus Foundation

Status

Completed

Conditions

Total Hip Replacement

Treatments

Device: Conventional physiotherapy
Device: Experimental group
Device: Control group

Study type

Interventional

Funder types

Other

Identifiers

NCT02861638
Hip Replacement

Details and patient eligibility

About

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.

Enrollment

30 patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

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);

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Experimental group
Experimental group
Description:
Video of the exercises and conventional physiotherapy. 30 minutes twice a day, 5 days a week for 2 weeks.
Treatment:
Device: Experimental group
Device: Conventional physiotherapy
Control group
Active Comparator group
Description:
Video of nature scenes and conventional physiotherapy. 30 minutes twice a day, 5 days a week for 2 weeks.
Treatment:
Device: Conventional physiotherapy
Device: Control group

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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