跳至主要内容
临床试验/NCT05699031
NCT05699031招募中不适用

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

University Hospital, Ghent2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2023年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
2
主要终点
SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline pre-operative

研究概览

简要总结

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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

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

结局指标

主要结局

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

时间窗: 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)

时间窗: 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

时间窗: 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

次要结局

  • 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)
  • GLOBAL PERCEIVED EFFECT (GPE/GEE)(Prior to surgery, week 3, week 6, week 12, week 52)
  • ACTIVE MOBILITY (ROM) OF THE SHOULDER(Prior to surgery, week 3, week 6, week 12, week 52)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验