- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00090961
S0229, Pulmonary Rehabilitation Education w/wo Exercise Training in Improving Physical Function in Patients Who Are Undergoing Chemo & RT for Locally Advanced Lung Cancer
A Randomized Trial Assessing the Effects of Exercise on Patients With Locally Advanced Lung Cancer Undergoing Curative Intent Combined Modality Therapy
RATIONALE: Pulmonary rehabilitation education and exercise training may improve physical function and quality of life in patients who are receiving treatment for lung cancer.
PURPOSE: This randomized clinical trial is studying pulmonary rehabilitation education and exercise training to see how well they work compared to exercise training alone in improving physical function and quality of life in patients who are undergoing chemotherapy and radiation therapy for locally advanced lung cancer.
연구 개요
상세 설명
OBJECTIVES:
- Compare improvement in physiologic function, in terms of exercise tolerance, in patients with inoperable locally advanced lung cancer undergoing chemoradiotherapy and randomized to pulmonary rehabilitation comprising education with vs without supervised exercise training.
- Compare the health-related quality of life, in terms of multidimensional functioning and patient perception of respiratory difficulties, in patients undergoing these pulmonary rehabilitation interventions.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to Zubrod performance status (0-1 vs 2); FEV_1 (≥ 70% of predicted vs < 70% of predicted); and smoking status* (never smoked or former smoker vs current smoker). Approximately 20 weeks into treatment on SWOG-S0023, patients are randomized to 1 of 2 intervention arms.
NOTE: * Never smoked is defined as < 100 cigarettes in a lifetime and former smoker is defined as no smoking for ≥ 1 year.
- Arm I: Patients participate in a supervised structured exercise program (i.e., walking on a treadmill OR using a stationary exercise bicycle) 3 times a week for 12 weeks. Patients also receive educational materials on how to improve breathing and conserve energy.
- Arm II: Patients receive educational materials as in arm I. In both arms, patients undergo exercise testing using 6-minute walks to measure exercise tolerance at initial evaluation (after randomization but prior to intervention), 12 weeks, and then at 6 and 9 months.
In both arms, intervention continues in the absence of disease progression or the development of other medical conditions that would preclude study participation.
Quality of life is assessed at baseline, 12 weeks, and then at 6 and 9 months.
PROJECTED ACCRUAL: A total of 164 patients (82 per treatment arm) will be accrued for this study.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Colorado
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Fort Collins, Colorado, 미국, 80524
- Poudre Valley Hospital
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Illinois
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Decatur, Illinois, 미국, 62526
- Decatur Memorial Hospital Cancer Care Institute
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Maywood, Illinois, 미국, 60153
- Cardinal Bernardin Cancer Center at Loyola University Medical Center
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Springfield, Illinois, 미국, 62781-0001
- Regional Cancer Center at Memorial Medical Center
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Kansas
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Chanute, Kansas, 미국, 66720
- Cancer Center of Kansas, PA - Chanute
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Dodge City, Kansas, 미국, 67801
- Cancer Center of Kansas, PA - Dodge City
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El Dorado, Kansas, 미국, 67042
- Cancer Center of Kansas, PA - El Dorado
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Independence, Kansas, 미국, 67301
- Cancer Center of Kansas-Independence
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Kingman, Kansas, 미국, 67068
- Cancer Center of Kansas, PA - Kingman
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Liberal, Kansas, 미국, 67901
- Southwest Medical Center
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Newton, Kansas, 미국, 67114
- Cancer Center of Kansas, PA - Newton
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Parsons, Kansas, 미국, 67357
- Cancer Center of Kansas, PA - Parsons
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Pratt, Kansas, 미국, 67124
- Cancer Center of Kansas, PA - Pratt
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Salina, Kansas, 미국, 67042
- Cancer Center of Kansas, PA - Salina
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Salina, Kansas, 미국, 67401
- Tammy Walker Cancer Center at Salina Regional Health Center
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Wellington, Kansas, 미국, 67152
- Cancer Center of Kansas, PA - Wellington
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Wichita, Kansas, 미국, 67208
- Cancer Center of Kansas, PA - Medical Arts Tower
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Wichita, Kansas, 미국, 67214
- Cancer Center of Kansas, PA - Wichita
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Wichita, Kansas, 미국, 67214
- CCOP - Wichita
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Wichita, Kansas, 미국, 67214
- Via Christi Cancer Center at Via Christi Regional Medical Center
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Wichita, Kansas, 미국, 67208
- Associates in Womens Health, PA - North Review
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Winfield, Kansas, 미국, 67156
- Cancer Center of Kansas, PA - Winfield
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Michigan
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Detroit, Michigan, 미국, 48201-1379
- Barbara Ann Karmanos Cancer Institute
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Mississippi
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Pascagoula, Mississippi, 미국, 39581
- Regional Cancer Center at Singing River Hospital
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Missouri
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Springfield, Missouri, 미국, 65802
- CCOP - Cancer Research for the Ozarks
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Springfield, Missouri, 미국, 65804
- St. John's Regional Health Center
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Springfield, Missouri, 미국, 65807
- Hulston Cancer Center at Cox Medical Center South
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Montana
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Billings, Montana, 미국, 59101
- CCOP - Montana Cancer Consortium
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Billings, Montana, 미국, 59101
- Hematology-Oncology Centers of the Northern Rockies - Billings
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Billings, Montana, 미국, 59101
- Northern Rockies Radiation Oncology Center
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Billings, Montana, 미국, 59101
- St. Vincent Healthcare Cancer Care Services
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Billings, Montana, 미국, 59107-7000
- Billings Clinic - Downtown
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Bozeman, Montana, 미국, 59715
- Bozeman Deaconess Cancer Center
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Butte, Montana, 미국, 59701
- St. James Healthcare Cancer Care
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Great Falls, Montana, 미국, 59405
- Great Falls Clinic - Main Facility
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Great Falls, Montana, 미국, 59405
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Great Falls, Montana, 미국, 59405-5309
- Big Sky Oncology
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Great Falls, Montana, 미국, 59405
- Sletten Cancer Institute at Benefis Healthcare
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Havre, Montana, 미국, 59501
- Northern Montana Hospital
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Helena, Montana, 미국, 59601
- St. Peter's Hospital
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Kalispell, Montana, 미국, 59901
- Kalispell Regional Medical Center
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Kalispell, Montana, 미국, 59901
- Glacier Oncology, PLLC
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Kalispell, Montana, 미국, 59901
- Kalispell Medical Oncology at KRMC
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Missoula, Montana, 미국, 59801
- Community Medical Center
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Missoula, Montana, 미국, 59804
- Guardian Oncology and Center for Wellness
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Missoula, Montana, 미국, 59807-7877
- Montana Cancer Specialists at Montana Cancer Center
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Missoula, Montana, 미국, 59807
- Montana Cancer Center at St. Patrick Hospital and Health Sciences Center
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North Carolina
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Goldsboro, North Carolina, 미국, 27534
- Wayne Memorial Hospital, Incorporated
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Washington
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Bellingham, Washington, 미국, 98225
- St. Joseph Cancer Center
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Bremerton, Washington, 미국, 98310
- Olympic Hematology and Oncology
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Kennewick, Washington, 미국, 99336
- Columbia Basin Hematology
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Seattle, Washington, 미국, 98104
- Harborview Medical Center
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Seattle, Washington, 미국, 98104
- Fred Hutchinson Cancer Research Center
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Seattle, Washington, 미국, 98104
- Minor and James Medical, PLLC
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Seattle, Washington, 미국, 98112
- Group Health Central Hospital
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Seattle, Washington, 미국, 98122-4307
- Swedish Cancer Institute at Swedish Medical Center - First Hill Campus
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Seattle, Washington, 미국, 98122
- Polyclinic First Hill
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Seattle, Washington, 미국, 98195-6043
- University Cancer Center at University of Washington Medical Center
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Spokane, Washington, 미국, 99202
- Cancer Care Northwest - Spokane South
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Wyoming
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Sheridan, Wyoming, 미국, 82801
- Welch Cancer Center at Sheridan Memorial Hospital
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참여기준
자격 기준
공부할 수 있는 나이
- 어린이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
DISEASE CHARACTERISTICS:
Histologically or cytologically confirmed single, primary bronchogenic lung cancer
- Inoperable, locally advanced disease (unresectable stage IIIA OR stage IIIB disease)
The following histologies are eligible:
- Adenocarcinoma
- Large cell carcinoma
- Squamous cell carcinoma
- Non-lobar and non-diffuse bronchoalveolar carcinoma
- Small cell lung cancer
Must have received chemotherapy (platinum based) and radiotherapy for locally advanced unresectable lung cancer
- Must have achieved a complete response, partial response, or stable disease after treatment
PATIENT CHARACTERISTICS:
Age
- Not specified
Performance status
- Zubrod 0-2
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Not specified
Renal
- Not specified
Cardiovascular
- No acute EKG changes, arrhythmia, or other cardiac abnormality that would preclude study participation
- No uncontrolled cardiac disease
- No recent myocardial infarction
Pulmonary
- Any FEV_1 level by pulmonary function testing
Other
- Willing to participate in 12-week long exercise program
- Chemotherapy-induced neuropathy ≤ grade 2
- No uncontrolled diabetes mellitus
- No other medical condition that would preclude study participation
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Not specified
Chemotherapy
- See Disease Characteristics
Endocrine therapy
- Not specified
Radiotherapy
- See Disease Characteristics
Surgery
- Not specified
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
---|---|
실험적: 12-week exercise program + education
A 12-week supervised exercise program consisting of 3 days a week on a stationary bike or treadmill.
In addition, at the time of enrollment patients are provided educational materials focusing on breathing and energy conservation.
|
|
다른: Education
At the time of enrollment patients are provided educational materials focusing on breathing and energy conservation.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Exercise tolerance
기간: Baseline and at 6 months
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comparison between the control and intervention arms in the percent change in the 6-minute walk distance between baseline and 6 months.
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Baseline and at 6 months
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Health-related quality of life
기간: Baseline and at 6 months.
|
The difference in total score between pre-study and 6 months for the FACT-L Quality of Life measure.
|
Baseline and at 6 months.
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공동 작업자 및 조사자
수사관
- 연구 의자: Antoinette J. Wozniak, MD, Barbara Ann Karmanos Cancer Institute
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 연구와 관련된 용어
기타 연구 ID 번호
- CDR0000380928
- U10CA012027 (미국 NIH 보조금/계약)
- SWOG-S0229
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. .
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Georgetown UniversityNational Cancer Institute (NCI); American Cancer Society, Inc.; Susan G. Komen Breast Cancer...완전한
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Assiut University아직 모집하지 않음South Egypt Cancer Institute(SECI)에서 소아 악성종양 환자에 대한 KDIGO 기준을 사용하여 AKI의 누적 발병률을 확인하기 위해
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VA Office of Research and Development모집하지 않고 적극적으로
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Washington University School of MedicineSt. Jude Children's Research Hospital완전한
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University of MichiganNational Institute on Drug Abuse (NIDA)모병
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The University of Hong KongResearch Grants Council, Hong Kong모집하지 않고 적극적으로
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RTI InternationalUniversity of North Carolina, Chapel Hill초대로 등록결절성 경화증 | 다운 증후군 | 뒤시엔 근이영양증 | 프래더-윌리 증후군 | 취약 X 증후군 | 레트 증후군 | 터너 증후군 | 윌리엄스 증후군 | 엔젤만 증후군 | 염색체 22q11.2 결실 증후군 | 클라인펠터 증후군 | 펠란-맥더미드 증후군 | Dup15Q 증후군 | 스미스 마제니스 증후군미국
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University of MichiganNational Institute of Nursing Research (NINR)완전한