베타
임상 레이더 AI
임상시험 NCT05035810 (MOVE-OK)은(는) 무릎 골관절염에 대해 진행중, 모집종료 상태입니다. 모든 세부 정보를 보려면 임상시험 레이더 카드 뷰와 AI 발견 도구를 확인하거나 여기에서 무엇이든 물어보세요.
하나의 임상시험이 필터 기준과 일치합니다.
카드 뷰

A Pragmatic Trial to Determine the Benefit of Behaviorally Enhanced Exercise Incentives and Corticosteroid Injections in Osteoarthritis of the Knee Marching On for Veterans With Osteoarthritis of the Knee (MOVE-OK)

진행중, 모집종료
임상시험 세부 정보는 주로 영어로 제공됩니다. 하지만 임상 레이더 AI가 도와드릴 수 있습니다! '시험 설명하기'를 클릭하여 선택한 언어로 임상시험 정보를 확인하고, 이에 대해 AI와 논의해 보세요.
임상시험 NCT05035810 (MOVE-OK)은(는) 치료을(를) 알아보기 위한 연구입니다. 이 연구는 무릎 골관절염에 대해 진행되며, 3상 중재연구으로 현재 상태는 진행중, 모집종료입니다. 연구는 2022년 3월 14일에 시작되어 221명의 참여자를 모집하고 있습니다. VA Office of Research and Development이(가) 진행하며, 2025년 12월 31일까지 완료될 예정입니다. ClinicalTrials.gov의 가장 최근 정보는 2025년 3월 20일에 갱신되었습니다.
간단한 개요
Knee osteoarthritis (KOA) is one of the most common and disabling conditions among Veterans. Management of KOA is challenging as there are few effective treatments other than joint replacement. Importantly, low levels of physical activity in patients with knee problems might worsen pain and disability. This study aims to determine the feasibility of using methods to change behavior that use social incentives and promote physical activity through playing games and interacting with a web-based platform. The study will also evaluate an important and widely used treatment, namely corticosteroid injections. Participants will be randomized into one of 4 arms and will receive a different combination of social incentives and injections. The study will evaluate which approach is most effective at promoting physical activity and reducing pain and disability.
상세한 설명
Knee osteoarthritis (KOA) is one of the most prevalent and disabling conditions among Veterans and accounts for high morbidity and high costs for the VA. Management of KOA is challenging as there are few consistently effective treatments other than joint replacement. Importantly, chronic reductions in physical activity in patients with KOA may worsen pain, physical function, and exacerbate the metabolic consequences of obesity. Moreover, the greater mortality observed in symptomatic knee OA populations is likely mediated through its effect on physical activity. The current proposal aims to derive preliminary data to support a large pragmatic trial testing the impact of interventions geared towards improving physical activity and function in KOA patients.

Promoting physical activity has been shown to be helpful in reducing pain and improving function in KOA and other groups. However, promoting behavioral change in the arthritis population is a significant challenge. The group has shown that social incentives [and gamification] derived from concepts from the field of behavioral economics to promote behavioral change and increase physical activity can be both practical and effective in other settings. The investigators' group is studying incentives in patients with inflammatory arthritis with the goal of addressing fatigue, pain, and deficits in physical function. The incentivization of physical activity using this approach represents a novel intervention for the managing symptoms of KOA and to improving overall health.

Analgesic therapies can help KOA patients participate in exercise therapy. However, whether corticosteroid injections, a commonly used medical therapy for KOA pain, has a positive impact of physical activity is unknown and is an additional important question addressed by the current proposal. Despite widespread use, definitive data demonstrating a consistent benefit of corticosteroids are lacking. A large randomized trial recently tested the effects of repeated corticosteroids injections every 3 months for a period of 2 years on patient reported pain as well as progression of disease measured by magnetic resonance imaging (MRI). This study demonstrated no improvement in pain compared to saline injections. In addition, a small but statistically significant decline in cartilage thickness on MRI was observed, raising a concern for side effects. These recent data might suggest that corticosteroid injections result in more harm than good, and may discourage providers from performing this intervention. However, there are critical weaknesses to this study. Pain and function were only assessed at 3-month intervals, while previous trials have suggested that peak benefit is expected at 4-8 weeks. Moreover, the clinical and biologic significance decrease in cartilage thickness is unclear.

The investigators propose to fill these important knowledge gaps with an innovative and efficient pragmatic clinical trial with a factorial and crossover design. A large and definitive practical trial would lead to better understanding of the clinical effectiveness of these interventions, the meaningfulness of their combined impact, and the subgroups that are most likely to derive benefit. This clinical trial will leverage unique resources available through the Penn Center for Innovation to better capture important patient-reported outcomes in real-time through a web-based platform. The study will also test the feasibility of a crossover and factorial design to improve efficiency and reduce confounding. Each patient will receive each intervention (saline, corticosteroids) in random order over 1 year. A factorial design will be employed and will randomize participants to receive social incentives with gamification to promote increases in their physical activity. To accomplish these aims, the investigators will utilize innovative mobile applications for smart phones and wearable activity trackers through the Way-to-Health platform and assess, in real time, the impact of the intervention on patient-reported function and pain as well as physical activity. The technology will allow for the recording of outcomes as they occur, between clinic visits, thereby avoiding information bias due to poor recall. It will also provide real-time assessment of symptoms, providing granular assessments of response over time.

Aim 1: To determine whether an incentive based on behaviorally-enhanced gamification can improve physical activity among patients with KOA and reduce self-reported pain and disability. The intervention will result in sustained improvements in average daily step counts over 10 months.

Aim 2: To determine if corticosteroid injections can reduce pain and disability in patients with KOA when compared to lidocaine only. Participants will report improvements in self-reported pain and disability, and improvements in quality of life.

공식 제목

A Pragmatic Trial to Determine the Benefit of Behaviorally Enhanced Exercise Incentives and Corticosteroid Injections in Osteoarthritis of the Knee

질환/상태
무릎 골관절염
출판물
이 임상 시험에 대해 발표된 과학 논문 및 연구 자료.
기타 연구 식별자
  • MOVE-OK
  • F3644-R
  • RX003644-01A1 (기타 보조금/자금 번호) (VA RR&D)
NCT 번호
실제 연구 시작일
2022-03-14
최신 업데이트 게시
2025-03-20
예상 연구 완료일
2025-12-31
계획된 등록 인원
221
연구종류
중재연구
단계/상
3상
상태
진행중, 모집종료
키워드
corticosteroid injection
physical activity
pain
disability
behavioral incentives
Osteoarthritis
Osteoarthritis, Knee
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
주요 목적
치료
설계 할당
무작위배정
중재 모델
요인설계
맹검 (마스킹)
이중맹검
시험군 / 개입
참가자 그룹/시험군개입/치료
실험적Social Incentives and Gamification, Corticosteroid AB
Participants will receive a support person and be able to interact with a web-based platform to progress through levels based on their achievement of step goals. The participants will receive injections in A-B order (corticosteroids, then lidocaine only)
Social Incentives and Gamification to Promote Exercise
The intervention will provide social incentives and gamification to promote physical activity.
Corticosteroid Injection Given in A-b Order
The study will compare corticosteroid injections with lidocaine to lidocaine only in a crossover design. These participants will receive the medication in A-B order.
활성 대조군No Incentive, Corticosteroid AB
Participants will only receive reminders to sync their activity monitor. The participants will receive injections in A-B order (corticosteroids, then lidocaine only)
Corticosteroid Injection Given in A-b Order
The study will compare corticosteroid injections with lidocaine to lidocaine only in a crossover design. These participants will receive the medication in A-B order.
No Social Incentive Applied
No social incentive will be applied
실험적Social Incentives and Gamification, Corticosteroid BA
Participants will receive a support person and be able to interact with a web-based platform to progress through levels based on their achievement of step goals. The participants will receive injections in B-A order (lidocaine only, then corticosteroids)
Social Incentives and Gamification to Promote Exercise
The intervention will provide social incentives and gamification to promote physical activity.
Procedure: Corticosteroid Injection Given in B-a Order
The study will compare corticosteroid injections with lidocaine to lidocaine only in a crossover design. These participants will receive the medication in B-A order.
활성 대조군No Incentive, Corticosteroid BA
Participants will only receive reminders to sync their activity monitor. The participants will receive injections in B-A order (lidocaine only, then corticosteroids)
No Social Incentive Applied
No social incentive will be applied
Procedure: Corticosteroid Injection Given in B-a Order
The study will compare corticosteroid injections with lidocaine to lidocaine only in a crossover design. These participants will receive the medication in B-A order.
주요결과변수
결과변수측정값 설명시간 범위
Percent change from baseline in weekly average steps per day
Steps measured by a wearable activity monitor
Measured weekly over 10 months (for exercise intervention)
Change in Knee Injury and Osteoarthritis Outcome Score (KOOS)
KOOS assessed by survey at 2 week intervals. KOOS scores range from 0 to 100 with 0 representing worse knee problems and 100 representing no knee problems.
Measured bi-weekly over the first 3 months (for injection intervention)
이차결과변수
결과변수측정값 설명시간 범위
Change in PROMIS pain intensity score
Assessed by survey at 2 week intervals. Scores range from 3-15 and are converted to T-Scores. A high score represents greater pain.
Measured bi-weekly over 3-10 months (3 for injection intervention and 10 for exercise intervention)
Change in PROMIS Fatigue
Assessed by survey at 4 week intervals
Measured every 4 weeks over 3-10 months (3 for injection intervention and 10 for exercise intervention)
Change in Knee Injury and Osteoarthritis Outcomes Score (KOOS)
KOOS assessed by survey at 2 week intervals. KOOS scores range from 0 to 100 with 0 representing worse knee problems and 100 representing no knee problems.
Measured bi-weekly over 10 months (for exercise intervention)
적격성 기준

연령대
성인, 노인
최소 연령
40 Years
참여 가능한 성별
전체
  • Veterans in VA Rheumatology or Orthopedic clinics
  • Chronic knee osteoarthritis
  • Indication for joint injection
  • Previous joint injections for palliation
  • Patient expresses interest in increasing their physical activity
  • Patient is able to walk 1/2 mile per day

  • Intra-articular hardware or other contraindication to joint injection
  • Lack of smart phone
  • Acute exacerbation of osteoarthritis or knee pain
  • Comorbid condition that precludes safe exercise
VA Office of Research and Development logoVA Office of Research and Development
연락처 정보가 없습니다.
4 1개국에 임상시험 장소

District of Columbia

Washington DC VA Medical Center, Washington, DC, Washington D.C., District of Columbia, 20422, United States

Nebraska

Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NE, Omaha, Nebraska, 68105-1873, United States

Pennsylvania

Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, Philadelphia, Pennsylvania, 19104-4551, United States

Washington

VA Puget Sound Health Care System Seattle Division, Seattle, WA, Seattle, Washington, 98108, United States