- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01136083
Effect of Exercise Training on Angiogenesis and Cachexia in Lung Cancer Patients
Cancer is one of the leading health issues in this country and worldwide. Angiogenesis is an essential process for tumoral growth and metastasis. This process is dependent on the balance between angiogenic factors and antiangiogenic factors. Muscle wasting has been associated with myostatin overexpression in cancer. Exercise training can depress tumor growth and suppress myostatin expression, and enhance skeletal muscle angiogenesis in healthy people and some animal studies. The purpose of this study is mainly to investigate the effects of exercise training on
- circulating VEGF-A
- muscle growth and function
- Myostatin
연구 개요
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Taipei City, 대만, 100
- National Taiwan University Hospital
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Age 40-75 years
- Advanced NSCLC
- Eastern Cooperative Oncology Group performance status of 0 or 1
- Targeted therapy for at least 8 weeks
- Stable condition
Exclusion Criteria:
- Severe metastasis, cardiopulmonary or musculoskeletal conditions may affect participation in exercise
- Do not understand the verbal or written instructions
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Exercise training
Subjects in exercise group will undergo individualized high aerobic interval training on treadmill for 30 minutes under the supervision of an experienced physical therapist 3 times a week and home exercise twice a week with accelerometer.
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Subjects in exercise group will undergo individualized high aerobic interval training on treadmill for 30 minutes under the supervision of an experienced physical therapist 3 times a week and home exercise twice a week with accelerometer.
다른 이름들:
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활성 비교기: Control group
Subjects in control group will not undergo individualized high aerobic interval training on treadmill.
They will receive usual care as normally does in hospital.
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Subjects in control group will not undergo individualized high aerobic interval training on treadmill.
They will receive usual care as normally does in hospital.
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Exercise capacity
기간: 8 weeks after the start of the intervention
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Maximal oxygen consumption with Vmax229 Vastus lateral muscle oxygenation with NIRS
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8 weeks after the start of the intervention
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Imaging of muscle
기간: 8 weeks and 16 weeks after the start of the intervention
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Measured by MRS
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8 weeks and 16 weeks after the start of the intervention
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Analysis of venous blood sample
기간: 8 weeks andd 16 weeks after the start of the intervention
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Analysis of circulating VEGF-A and myostatin
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8 weeks andd 16 weeks after the start of the intervention
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Quality of life
기간: baseline, 8 weeks, 16 weeks
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Measured by questionnaire
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baseline, 8 weeks, 16 weeks
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Exercise capacity
기간: 16 weeks after the start of the intervention
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Maximal oxygen consumption with Vmax229 Vastus lateral muscle oxygenation with NIRS
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16 weeks after the start of the intervention
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Muscle function
기간: 8 weeks and 16 weeks after the start of the intervention
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Isokinetic muscle strength and endurance with Biodex
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8 weeks and 16 weeks after the start of the intervention
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Physical activity
기간: 8 weeks andd 16 weeks after the start of the intervention
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Measured with 7-day recall questionnaire
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8 weeks andd 16 weeks after the start of the intervention
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Dietary intake
기간: 8 weeks andd 16 weeks after the start of the intervention
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Measured with 24-hour recall questionnaire
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8 weeks andd 16 weeks after the start of the intervention
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Body composition
기간: 8 weeks andd 16 weeks after the start of the intervention
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Body mass index calculated with body weight and height % body fat abd free-fat mass with BIA |
8 weeks andd 16 weeks after the start of the intervention
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .