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临床试验/NCT06101797
NCT06101797已完成不适用

Remote and In-person Supervised Exercise in Patients With Knee Osteoarthritis (RISE-KOA): a Single Blinded, Randomized, Non-inferiority Trial.

Federal University of Pelotas2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2023年12月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
试验地点
2
主要终点
Pain intensity

研究概览

简要总结

Exercise supervision via telehealth resources is an alternative to the in-person modality with similar therapeutic effectiveness across different clinical profiles. Especially in the context of knee osteoarthritis (OA), exercise is recommended by international guidelines. However, it is necessary to elucidate the comparability of remote and in-person supervised exercise effectiveness for these patients. Therefore, the study's objective is to investigate the responses of a remote compared to the in-person supervised exercise program on patient-reported outcomes measures (PROMs), muscular architecture, and the functional performance of patients with knee OA. Forty-eight patients with symptomatic and radiographic knee OA will be randomly assigned to remote or in-person exercise programs. The intervention will last 12 weeks, encompassing muscle-strengthening exercises for the lower extremities, with a frequency of twice a week for the initial two weeks and three sessions per week from the third week onwards. Supervision will be conducted remotely via video calls in one group, while the other will receive in-person supervision at a physiotherapy clinic. Program sessions will comprise six exercises. In the first session treatment block, exercises will be guided for the muscle groups of the knee extensors, hip adductors, and plantar flexors, and in the second block, for knee extensors, hip abductors, and knee flexors. After the 12-week supervised treatment period, participants will be encouraged to continue the same exercise program at home without a physiotherapist in the following six weeks. PROMs related to the joint condition will be measured, such as pain, symptoms, daily activities, sports and leisure activities, and quality of life. The psychological domain will also be evaluated, including pain catastrophizing, symptoms of depression, anxiety and stress, and sleep quality. Additionally, measurements of the muscular architecture of the quadriceps femoris, including muscle thickness, pennation angle, fascicle length, and echo intensity, will be taken. Functional performance will be assessed through tests that include the skills of standing and sitting, walking and going up, and down stairs. PROMs will be measured at weeks 0, 6, 12, and 18. Muscular architecture and functional parameters will be measured at weeks 0 and 12. Data analysis will be conducted using Linear Mixed Models, and analysis will be presented by intention to treat and per protocol. The significance level adopted for this study will be α = 0.05.

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)

盲法说明

Blinding will be implemented by the outcome assessor. All measurements (PROMs, muscle architecture, and functional outcomes) will be conducted by an evaluator blinded to the participant's group. Due to the nature of the intervention, investigators conducting the exercise intervention and participants will not be able to be blinded.

入排标准

年龄范围
45 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with a radiographic diagnosis of unilateral or bilateral knee OA and classified as grades II or III according to the Kellgren and Lawrence criteria (KELLGREN e LAWRENCE, 1957).
  • Symptomatic patients according to following American College of Rheumatology criteria - average pain score ≥3 in the last week on the numerical rating scale (0-10), morning stiffness <30 minutes and joint crepitus (ALTMAN et al., 1986).
  • Independent walking and internet access.

排除标准

  • Patients with systemic inflammatory diseases, including rheumatoid arthritis, ankylosing spondylitis, and systemic lupus erythematosus.
  • Neurological diseases with motor disability.
  • Unstable heart diseases.
  • History of total knee arthroplasty or lower extremity surgery.
  • Body mass index (BMI) ≥ 35 kg/m².
  • Physical therapy treatment or participation in a supervised exercise program in the last six months.

结局指标

主要结局

Pain intensity

时间窗: Baseline (week 0), During intervention (week 6), Post-intervention (week 12).

Average pain intensity in the last week will be assessed using an 11-point Pain Intensity Numerical Rating Scale (NRS), in which 0 corresponds to "no pain," and 10 represents "worst possible pain." NRS is a patient-reported outcome measure for assessment and clinical decision-making in patients with knee OA with good psychometric properties (ORNETTI et al., 2011).

Physical function

时间窗: Baseline (week 0), During intervention (week 6), Post-intervention (week 12).

Physical function will be measured by Knee Injury and Osteoarthritis Outcome Score (KOOS) using an Activities of Daily Living subscale. The KOOS is a patient-reported outcome measure composed of 42 items divided into five subscales: Pain, other Symptoms, Activities of daily living, Sport and Recreation Function, and Knee-related Quality of Life. Its score ranges from 0 (extreme problem) to 100 (no problems) separately in each subscale (COLLINS et al., 2011). The Brazilian version of the KOOS questionnaire was recently validated, consisting of an instrument with validity, reliability, and responsiveness in patients with knee OA (ALMEIDA et al., 2022).

次要结局

  • Pain intensity(Follow up period (week 18).)
  • Physical function(Follow up period (week 18).)
  • Pain score(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Other Symptoms(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Sport and Recreation Function(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Knee-related Quality of Life(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Pain catastrophizing(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Symptoms of depression, anxiety, and stress(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Sleep quality(Baseline (week 0), During intervention (week 6), Post-intervention (week 12), Follow up period (week 18).)
  • Sit-to-stand activity(Baseline (week 0), and Post-intervention (week 12).)
  • Ambulatory transition activity(Baseline (week 0), and Post-intervention (week 12).)
  • Short distance walking activity(Baseline (week 0), and Post-intervention (week 12).)
  • Stair negotiation activity(Baseline (week 0), and Post-intervention (week 12).)
  • Quadriceps femoris muscle thickness(Baseline (week 0), and Post-intervention (week 12).)
  • Quadriceps femoris muscle quality(Baseline (week 0), and Post-intervention (week 12).)
  • Pennation angle(Baseline (week 0), and Post-intervention (week 12).)
  • Fascicle length(Baseline (week 0), and Post-intervention (week 12).)

研究者

发起方
Federal University of Pelotas
申办方类型
Other
责任方
Principal Investigator
主要研究者

Cristine Lima Alberton

Principal Investigator

Federal University of Pelotas

研究点 (2)

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