- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT02628795
Overcoming TWEAK Signaling to Restore Muscle and Mobility After Joint Replacement (TWEAK)
2021년 7월 3일 업데이트: Marcas M. Bamman, PhD, University of Alabama at Birmingham
This single-blind, randomized, controlled trial is designed to test the effect of an intensive, 16 week exercise rehabilitation program (progressive resistance training + functional mobility training) vs. usual care on restoration of muscle mass and mobility after total hip (THA) or knee (TKA) arthroplasty in men and women with end-stage osteoarthritis.
The molecular basis underlying the trial is the presence of significant muscle inflammation susceptibility in many of these individuals, and the expectation that the more intensive intervention will overcome this inflammatory burden to facilitate recovery.
연구 개요
상세 설명
While elective total hip (THA) and knee (TKA) arthroplasty relieve pain and improve mobility function for thousands with end-stage osteoarthritis (OA), up to 35% endure persistent muscle atrophy and mobility limitations for several years that impact life quality, increase morbidity, and burden the healthcare system.
Given that THA/TKA volumes are increasing exponentially with >1.1 million in the US annually, refractory mobility impairment is a major public health problem.
Together, the available data raise two important knowledge gaps in THA/TKA rehabilitation: (i) poorly understood factors that limit responsiveness of a large number of patients to current usual care; and (ii) the absence of rehabilitation programs proven to overcome these limitations.
The proposed project is designed to fill these gaps.
The investigators' fundamental tenet is that restoration of mobility function following THA/TKA requires: (i) regeneration of surgically damaged muscle; and (ii) regrowth of muscles that have atrophied over years of OA and limited usage.
The investigators suggest a major cause of muscle regeneration impairment in some individuals is what the investigators identified as muscle inflammation susceptibility (MuIS) - hyperactive inflammatory signaling in muscle of MuIS(+) individuals despite no systemic inflammation - which also manifests in isolated primary satellite cells and inhibits myogenesis in vitro, indicative of a true cellular phenotype beyond the niche.
The investigators' preliminary findings in THA/TKA patients strongly suggest the tumor necrosis factor-like weak inducer of apoptosis (TWEAK) signaling pathway may be central to MuIS and impaired THA/TKA recovery, as high perioperative muscle TWEAK signaling in the ipsilateral thigh was the most sensitive indicator of impaired muscle protein synthesis and failed strength recovery after 8 wk of usual care.
Progressive resistance exercise training (PRT) is a putative anabolic intervention that the investigators find consistently increases muscle mass to meet healthy standards in atrophied and mobility-impaired adults, by activating muscle protein synthesis and the myogenic activity of muscle satellite cells.
Together, these findings raise the central hypothesis that PRT plus adjunctive functional mobility training (PRT+FM) after THA/TKA will more effectively restore muscle mass and mobility function to healthy standards than usual care and, because MuIS(+) are predicted to suffer failed muscle recovery and persistent dismobility under usual care, the impact of PRT+FM will be greatest in MuIS(+).
The investigators will thoroughly test this hypothesis in a randomized controlled trial of 88 THA/TKA patients with the following aims.
Aim 1: To determine the effects of 16 wk of PRT+FM vs. usual care after elective THA/TKA on muscle mass, performance, and mobility function.
Aim 2: To determine whether MuIS status modifies the effects of PRT+FM or usual care after THA/TKA.
Cellular and molecular mechanisms of muscle mass regulation will be studied in detail.
Aim 3. To determine the long-term impact of 16 wk PRT+FM by re-assessing outcomes at 6 mo and 1 y.
The investigators fully expect the novel findings to lead a paradigm shift in THA/TKA rehabilitation that will have a profound impact on a growing segment of the population.
연구 유형
중재적
등록 (실제)
80
단계
- 해당 없음
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Alabama
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Birmingham, Alabama, 미국, 35205
- UAB Center for Exercise Medicine
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
40년 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
Between the ages 40 and 80 y.
- Scheduled to undergo elective total hip or knee replacement specifically for the surgical indication of end-stage osteoarthritis.
- First-time hip or knee replacement.
- Capable of providing informed consent (cognitively intact if consenting to surgery).
Exclusion Criteria:
Any surgical indication other than first-time total joint replacement specifically for end-stage osteoarthritis.
- Bilateral knee/ hip replacement
- History of alcoholism or liver disease.
- Any history of hypo- or hyper-coagulation disorders including subjects taking Coumadin.
- Any individual with end-stage disease and/or a life expectancy less than one year.
- Pregnancy.
- Lactating Women.
- Neurological, musculoskeletal, or other disorder that would preclude them from completing the exercise training intervention and all performance tests.
- Uncontrolled hypertension, unstable or exercise-induced angina pectoris or myocardial ischemia, congestive heart failure.
- Uncontrolled diabetes mellitus.
- Any other condition or events considered exclusionary by the PIs and/or physician Co-Is.
- Lidocaine allergy (1% lidocaine is the local anesthetic used during the muscle biopsy procedure).
- Phenylketonuria (phenylalanine tracer for metabolic studies).
- Currently receiving androgen (e.g., testosterone) or anabolic (e.g., growth hormone (GH), insulin-like growth factor-I (IGF-I)) therapy.
- Body mass index ≥ 35.
- History of lower body progressive resistance training within the past year.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: PRT + FM
Progressive resistance training + functional mobility training 3 d/wk x 16 wk
|
Supervised progressive resistance training + functional mobility training (PRT+FM) 3 days per week for 16 weeks post-surgery.
Post-surgical usual care activities including any prescribed physical therapy
|
|
활성 비교기: Usual Care
Post-surgical usual care including physical therapy
|
Post-surgical usual care activities including any prescribed physical therapy
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in unilateral (surgical) thigh muscle mass (unit of measure = grams)
기간: Pre-surgery to 16 weeks post-surgery
|
Primary muscle mass outcome of Aim 1
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Pre-surgery to 16 weeks post-surgery
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Change in unilateral (surgical) knee extension power (unit of measure = watts)
기간: Pre-surgery to 16 weeks post-surgery
|
Primary functional outcome of Aim 1
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Pre-surgery to 16 weeks post-surgery
|
|
Change in short physical performance battery (SPPB) (unit of measure = score)
기간: From 16 weeks post-surgery to 26 and 52 weeks post-surgery
|
Primary outcome of Aim 3
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From 16 weeks post-surgery to 26 and 52 weeks post-surgery
|
|
Muscle inflammation susceptibility (MuIS) status (unit of measure = relative value)
기간: At the time of surgery
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Primary outcome of Aim 2: Muscle inflammation susceptibility (MuIS) defined by TWEAK receptor gene expression
|
At the time of surgery
|
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
Change in muscle fiber size (unit of measure = micrometers squared)
기간: From the time of surgery to 16 weeks post-surgery
|
From the time of surgery to 16 weeks post-surgery
|
|
Change in unilateral (surgical) knee extension isometric strength (unit of measure = Newton-meters)
기간: Pre-surgery to 16 weeks post-surgery
|
Pre-surgery to 16 weeks post-surgery
|
|
Change in maximum 10-meter gait speed (unit of measure = meters per second)
기간: Pre-surgery to 16 weeks post-surgery
|
Pre-surgery to 16 weeks post-surgery
|
기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in free-living physical activity (unit of measure = steps per day)
기간: Pre-surgery to 8, 16, 26, and 52 weeks post-surgery
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Via wearable technology (i.e.
step counter)
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Pre-surgery to 8, 16, 26, and 52 weeks post-surgery
|
|
Change in self-reported health status (unit of measure = score)
기간: Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
Via Short Form-36v2 Health Survey (SF-36v2)
|
Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
|
Change in cellular and molecular markers (unit of measure = arbitrary units)
기간: From the time of surgery to 16 weeks post-surgery
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Experiments using muscle tissue and primary muscle satellite cells collected from surgical and contralateral limbs.
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From the time of surgery to 16 weeks post-surgery
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Change in fatigue (unit of measure = score)
기간: Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
Via Patient Reported Outcomes Measurement Information System (PROMIS)
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Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
|
Change in pain (unit of measure = score)
기간: Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
Via Patient Reported Outcomes Measurement Information System (PROMIS)
|
Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
|
Change in depression (unit of measure = score)
기간: Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
Beck Depression Inventory (BDI II)
|
Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
|
Change in fatigue severity (unit of measure = score)
기간: Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
Fatigue Severity Scale (FSS)
|
Pre-surgery to 1, 8, 16, 26, and 52 weeks post-surgery
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
협력자
수사관
- 수석 연구원: Marcas M Bamman, PhD, University of Alabama at Birmingham
- 수석 연구원: S Louis Bridges, MD, PhD, University of Alabama at Birmingham
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2015년 10월 1일
기본 완료 (실제)
2020년 9월 1일
연구 완료 (실제)
2021년 2월 28일
연구 등록 날짜
최초 제출
2015년 8월 5일
QC 기준을 충족하는 최초 제출
2015년 12월 10일
처음 게시됨 (추정)
2015년 12월 11일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2021년 7월 7일
QC 기준을 충족하는 마지막 업데이트 제출
2021년 7월 3일
마지막으로 확인됨
2021년 7월 1일
추가 정보
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