跳至主要内容
临床试验/NCT05772715
NCT05772715已完成不适用

The THumb Osteoarthritis Exercise TriAl (THETA); a Multicenter, Randomized Controlled Trial on Exercise Therapy with an Orthosis Compared to an Orthosis Alone in Patients with Thumb Base Osteoarthritis

Erasmus Medical Center10 个研究点 分布在 1 个国家目标入组 166 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
166
试验地点
10
主要终点
Pain - change

研究概览

简要总结

THIS TRIAL WAS PROSPECTIVELY REGISTERED ON FEBRUARY 27, 2020 IN THE DUTCH TRIAL REGISTRY (www.trialregister.nl), BUT THIS TRIAL REGISTRY WAS TERMINATED. THE DATA ON OUR TRIAL WERE TRANSFERED BY THE DUTCH TRIAL REGISTRY TO WHO'S CLINICAL TRIALS SEARCH PORTAL (REFERENCE NUMBER: NL-OMON54664). WE ALSO REGISTERED THE TRIAL HERE AT CLINICALTRIALS.GOV TO BE ABLE TO ADD MORE DETAILS ON OUR STUDY.

Summary:

OBJECTIVE(S)/RESEARCH QUESTION(S) Does an orthosis combined with exercise therapy results in less pain and less conversion to surgery than an orthosis alone in patients with first carpometacarpal osteoarthritis (CMC-1 OA), at three months and one year after the start of treatment? HYPOTHESIS The investigators hypothesize that the orthosis + exercise therapy group has less pain and conversion to surgery will be lower than the orthosis group.

STUDY DESIGN Randomized controlled multicenter trial STUDY POPULATION(S)/DATASETS Patients with first carpometacarpal osteoarthritis (CMC-1 OA) seeking treatment INTERVENTION Orthosis + exercise therapy USUAL CARE/COMPARISON Orthosis only OUTCOME MEASURES Primary outcomes: pain and conversion to surgery SAMPLE SIZE CALCULATION/DATA ANALYSIS Two groups of 80 participants; analysis based on repeated measures analysis (for pain) and Chi-square tests (for conversion to surgery). The investigators initially planned to perform a survival analysis (log-rank) and logistic regression for conversion to surgery but decided prior to data analysis on using chi-square tests to determine whether there is a between-group difference in the proportion of conversion to surgery. The investigators made this decision due to low inclusion rates, as chi-square tests require smaller sample sizes. The investigators will use a mixed-effect model analysis for pain.

COST-EFFECTIVENESS ANALYSIS (CEA)/ BUDGET IMPACT ANALYSIS (BIA) Economic evaluation will be done from societal & healthcare perspectives, according cost-effectiveness analysis (CEA) guidelines. Medical & non-medical costs and consequences (i.e. productivity loss) will be collected and taken into account. Both CEA and cost-utility analysis will be performed, using conversion to surgery and Quality-adjusted life years (QALYs), respectively TIME SCHEDULE Start preparation: December 2019, inclusion: October 2020- December 2022, final report: December 2023

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
Double (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Pain - change

时间窗: 3 months (primary), other Time points: baseline, 6 weeks, 6 months, 1 year.

Michigan Hand Outcomes Questionnaire

Conversion to surgical treatment

时间窗: 12 months

Questionnaire: surgery yes/no

次要结局

  • Hand Function(Time points: baseline, 6 weeks, 3 months, 6 months, 1 year.)
  • Satisfaction with treatment results(Time points: 6 weeks, 3 months, 6 months, 1 year.)
  • Treatment adherence(Time points: 6 wks, 3 months)
  • Depression(Time points: baseline,3 months.)
  • Experience with healthcare delivery(Time points: 6 weeks, 3 months.)
  • Costs and productivity loss(Time points: 6 weeks, 3 months, 6 months, 9 months, 1 year.)
  • Perceived attention/quality of the relationship(Time points: 6 weeks, 3 months.)
  • Anxiety(Time points: baseline, 3 months.)
  • Pain catastrophizing(Time points: baseline.)
  • Return to work(Time points: 6 weeks, 3 months, 6 months, 9 months, 1 year.)
  • Grip & Pinch strength(Time points: baseline, 6 weeks, 3 months, 6 months, 1 year.)
  • Complications(Time points: baseline, 6 weeks, 3 months, 6 months, 1 year.)
  • Illness perception(Time points: baseline, 3 months.)
  • Treatment credibility and expectations(Time points: baseline, 6 weeks.)
  • Health-related quality of life(Time points: baseline, 6 weeks, 3 months, 6 months, 1 year.)
  • Range of motion(Time points: baseline, 6 weeks, 3 months, 6 months, 1 year.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Robbert Wouters

Dr. Robbert Wouters

Erasmus Medical Center

研究点 (10)

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