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Evaluation of Teleconsulting on Rehabilitation After Hip and Knee Surgical Procedures (SSRHAD)

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ClinicalTrials.gov Identifier: NCT02229279
Recruitment Status : Unknown
Verified January 2017 by Assistance Publique - Hôpitaux de Paris.
Recruitment status was:  Active, not recruiting
First Posted : September 1, 2014
Last Update Posted : January 11, 2017
Sponsor:
Collaborator:
Agence Regionale de Sante d'Ile de France
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris

Brief Summary:
The objective of this study is to assess the medical and economic relevance of teleconsulting for Rehabilitation After Hip and Knee Surgical Procedures.

Condition or disease Intervention/treatment Phase
Osteoarthritis, Hip Osteoarthritis, Knee Device: Teleconsulting Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 430 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Evaluation of Teleconsulting on Rehabilitation After Hip and Knee Surgical Procedures
Study Start Date : September 2015
Actual Primary Completion Date : October 2016
Estimated Study Completion Date : March 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Rehabilitation

Arm Intervention/treatment
Active Comparator: Teleconsulting
Teleconsulting
Device: Teleconsulting
Other Name: Telemedicine

No Intervention: No Teleconsulting



Primary Outcome Measures :
  1. Functional subscore of simplified WOMAC Scale [ Time Frame: up to 30 days after start of rehabilitation ]

Secondary Outcome Measures :
  1. Joint Paint measured with visual analogue scale [ Time Frame: up to 30 days after start of rehabilitation ]
  2. Patient satisfaction questionnaire [ Time Frame: The last 1 day of the rehabilitation ]
  3. Medical and paramedical staff satisfaction questionnaire [ Time Frame: 6 months after enrollment of the first patient ]
  4. Overall costs of treatment [ Time Frame: 6 months after enrollment of the first patient ]
  5. Number of hospitalizations and use of emergency units [ Time Frame: Within 30 days after start of rehabilitation ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Post hip or knee surgery
  • Fulfilment of criteria for home rehabilitation (no need for hospital treatment post surgery)

Exclusion Criteria:

  • Social isolation
  • Life threatening condition
  • No GSM network
  • No DSL network

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02229279


Locations
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France
Fondation Santé Service, Pôle Rééducation- Handicap
Puteaux, France, 92816
Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris
Agence Regionale de Sante d'Ile de France
Investigators
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Principal Investigator: Dominique Copin, MD Fondation Santé Service, Pôle Rééducation - Handicap
Principal Investigator: Isabelle Durand-Zaleski, MD, PhD DRCD URC Eco. Assistance Publique - Hôpitaux de Paris

Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier: NCT02229279     History of Changes
Other Study ID Numbers: TLM-HAD
First Posted: September 1, 2014    Key Record Dates
Last Update Posted: January 11, 2017
Last Verified: January 2017
Keywords provided by Assistance Publique - Hôpitaux de Paris:
Surgical Procedures, Operative
Additional relevant MeSH terms:
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Osteoarthritis
Osteoarthritis, Knee
Osteoarthritis, Hip
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases