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Clinical Trials/NCT05699031
NCT05699031RecruitingNot Applicable

The PROTECT-study: Home-based Telerehabilitation in the Post-operative Care After Shoulder Arthroplasty Compared to Usual Care: a Randomized Control Trial

University Hospital, Ghent1 site in 1 country120 target enrollmentStarted: March 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
120
Locations
1
Primary Endpoint
SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline pre-operative

Study Overview

Brief Summary

The goal of this clinical trial is to compare the rehabilitation by use of a smartphone-app with the usual care of physical therapy in patients, 60 years and older, who underwent a primary shoulder arthroplasty.

The main questions it aims to answer are:

  • is the outcome of rehabilitation with the app as good as the usual care?
  • is the outcome for both types of shoulder arthroplasty similar?
  • what is the usability of the app?.

Participants will

  • have treatment according to the group they are allocated to
  • fill in questionnaires at specific moments during the rehabilitation stage (0 - 3 months ) and at 1 year post-surgery

Study Design

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

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •60 years and older
  • •primary total shoulder arthroplasty (anatomical and reverse)
  • •osteoarthritis, cuff tear arthropathy, pseudoparalysis
  • •return home after discharge from hospital
  • •no brace after surgery
  • •sufficient verbal and written comprehension
  • •hospitalization insurance

Exclusion Criteria

  • •revision arthroplasty
  • •arthroplasty for fracture or tumor
  • •neurological disease (parkinson, stroke, ...)
  • •no access to smartphone, tablet or internet connectivity

Arms & Interventions

PHYSIO-GROUP

Active Comparator

Patients allocated in the physio-group will rehabilitate according to the usual care protocol

Intervention: PHYSICAL THERAPY (Other)

APP-GROUP

Experimental

Patients allocated in the app-group will use the app to rehabilitate.

Intervention: APP (Device)

Outcomes

Primary Outcomes

SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline pre-operative

Time Frame: Prior to surgery

Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

SHOULDER PAIN AND DISABILITY INDEX (SPADI)

Time Frame: week 52

Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline post-operative

Time Frame: week 0

Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

SHOULDER PAIN AND DISABILITY INDEX (SPADI)

Time Frame: week 3

Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

SHOULDER PAIN AND DISABILITY INDEX (SPADI)

Time Frame: week 6

Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

SHOULDER PAIN AND DISABILITY INDEX (SPADI)

Time Frame: week 12

Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

Secondary Outcomes

  • ACTIVE MOBILITY (ROM) OF THE SHOULDER(Prior to surgery, week 3, week 6, week 12, week 52)
  • GLOBAL PERCEIVED EFFECT (GPE/GEE)(Prior to surgery, week 3, week 6, week 12, week 52)
  • PASSIVE MOBILITY (ROM) OF THE SHOULDER(Prior to surgery, week 3, week 6, week 12, week 52)
  • STRENGTH(Prior to surgery, week 3, week 6, week 12, week 52)
  • CONSTANT-MURLEY SCORE(Prior to surgery, week 3, week 6, week 12, week 52)
  • ACTIVITIES OF DAILY LIVING EXTERNAL AND INTERNAL ROTATIONS (ADLEIR)(Prior to surgery, week 3, week 6, week 12, week 52)
  • EUROQOL 5-DIMENSIONS 5-LEVEL (EQ-5D-5L)(Prior to surgery, week 3, week 6, week 12, week 52)
  • SINGLE ASSESSMENT NUMERIC EVALUATION (SANE)(Prior to surgery, week 3, week 6, week 12, week 52)
  • GRONINGEN ACTIVITY RESTRICTION SCALE (GARS-4)(Prior to surgery, week 3, week 6, week 12, week 52)
  • EXERCISE ADHERENCE RATING SCALE (EARS)(Prior to surgery, week 3, week 6, week 12, week 52)
  • EXERCISE DIARY(Daily post-surgery (week 0 - week 12))
  • SELF-EFFICACY FOR EXERCISES (SEE)(Week 3, week 6, week 12, week 52)
  • GLOBAL RATING OF CHANGE SCALE (GROC)(Prior to surgery, week 3, week 6, week 12, week 52)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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