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OpenTrials
Completed

NCT Number: NCT02861638

Action Observation in Hip Replacement

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.

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Key information

Conditions

Total Hip Replacement

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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);

Treatment and study plan

Experimental Group

Device

Video of the exercises

Control group

Device

video of nature scenes

Conventional physiotherapy

Device

Mobilization, exercises and transfer practice.

Primary outcomes

  1. Change of Pain intensity

    Time frame: Baseline and immediately post-intervention

    Visual Analogue Scale (VAS)

  2. Change of Range Of Motion (ROM)

    Time frame: Baseline and immediately post-intervention

    Active and passive range of motion of hip

Secondary outcomes

  1. Barthel index

    Time frame: Baseline and immediately post-intervention

    Barthel Index of Activities of Daily Living

  2. Short Form-36 motor

    Time frame: Baseline and immediately post-intervention

    The Medical Outcome Study 36-Item Short Form Health Survey (SF-36) is a widely used method to evaluate health-related quality of life

  3. Tinetti scale

    Time frame: Baseline and immediately post-intervention

    Balance

  4. Lequesne index

    Time frame: Baseline and immediately post-intervention

    The Lequesne Index is a 10-question survey given to patients with osteoarthritis of the knee

Sponsors and collaborators

Lead sponsor

Fondazione Don Carlo Gnocchi ETS

Other

Registry information

Official study title

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

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Aug 10, 2016
Registry last updated
Aug 12, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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