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Effectiveness of Telerehabilitation Program in Subacromial Syndrome (Telerehab Sis)

NCT02909920 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 138

Last updated 2016-10-11

No results posted yet for this study

Summary

Shoulder pain is a common and high prevalence in the general population. Subacromial Syndrome (Shoulder Impingement Syndrome (SIS)) is the most frequent cause. SIS patients suffering pain, muscle weakness and loss of movement in the affected joint. Initial treatment of the SIS is predominantly conservative. Surgical option has high success rates and is often used when conservative strategy fails. Traditional Physiotherapy and Postoperative exercises is needed to the recovery of joint range, muscle strength, stability and functionality. This Research evaluates the feasibility and effectiveness of a telerehabilitatión Program in SIS after surgery compared with traditional therapy.

Conditions

  • Shoulder Impingement Syndrome

Interventions

OTHER

Telerehabilitation

Initial Videoconference following telerehabilitation programs self-workout exercise with video support.

OTHER

Traditional Physiotherapy

Traditional Physiotherapy receives assistance in a physiotherapy center with personalized therapy consisting of 1 to 1 with a physical therapist (Manual Therapy, home exercise programs and other physiotherapy techniques).

Sponsors & Collaborators

  • University of Malaga

    collaborator OTHER

  • Hospital Costa del Sol

    collaborator OTHER

  • Jose Manuel Pastora Bernal

    lead OTHER

Principal Investigators

  • Jose Manuel Pastora Bernal · University of Malaga

  • Rocio Martín Valero · University of Malaga

  • Francisco Javier Barón López · University of Malaga

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2017-03-31
Completion
2017-05-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02909920 on ClinicalTrials.gov