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Cancer Survivor clinical trials

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NCT ID: NCT00662103 Completed - Breast Cancer Clinical Trials

Aerobic Exercise, Resistance Exercise, or Flexibility and Relaxation Training in Inactive Older Female Breast Cancer Survivors

Start date: March 2008
Phase: N/A
Study type: Interventional

RATIONALE: Aerobic exercise, resistance exercise, and flexibility and relaxation training may reduce fatigue and improve the health and quality of life of breast cancer survivors. It is not yet known which type of exercise is more effective for inactive older female breast cancer survivors. PURPOSE: This randomized clinical trial is studying aerobic exercise to see how well it works compared with resistance exercise or flexibility and relaxation training in improving the health and quality of life of inactive older female breast cancer survivors.

NCT ID: NCT00336089 Recruiting - Breast Cancer Clinical Trials

Exercise Program or Health Education Program in Reducing Fatigue and Pain in Breast Cancer Survivors

Start date: January 2006
Phase: N/A
Study type: Interventional

RATIONALE: An exercise program or health education program may help relieve fatigue and pain and improve the quality of life in women who are breast cancer survivors. It is not yet known whether an exercise program is more effective than a health education program or no program in reducing fatigue and pain in women who are breast cancer survivors. PURPOSE: This randomized clinical trial is studying an exercise program to see how well it works in reducing fatigue and pain compared to a health education program or no program in women who are breast cancer survivors.

NCT ID: NCT00309933 Completed - Breast Cancer Clinical Trials

Quality of Life in Female Breast Cancer Survivors and Their Spouse, Partner, or Acquaintance

Start date: April 3, 2006
Phase:
Study type: Observational

RATIONALE: Studying quality of life in breast cancer survivors may help determine the long-term effects of breast cancer and may help improve the quality of life for future breast cancer survivors. PURPOSE: This clinical trial is studying quality of life in female breast cancer survivors and their spouse, partner, or acquaintance.

NCT ID: NCT00268502 Completed - Breast Cancer Clinical Trials

Quality of Life in African-American or Caucasian Female Breast Cancer Survivors

Start date: December 2005
Phase: N/A
Study type: Observational

RATIONALE: Studying quality of life in cancer survivors may help determine the long-term effects of breast cancer and may help improve the quality of life for future cancer survivors. PURPOSE: This clinical trial is studying the quality of life in African-American or Caucasian female breast cancer survivors.

NCT ID: NCT00246818 Completed - Cancer Clinical Trials

Effect of Tai Chi Vs. Structured Exercise on Physical Fitness and Stress in Cancer Survivors

Start date: October 26, 2005
Phase: Phase 2
Study type: Interventional

This study will compare the effectiveness of Tai Chi (a sequence of slow, graceful body movements) and a cardiovascular exercise fitness program in improving physical fitness and endurance, reducing stress and improving well-being in adult survivors of cancer. Tai Chi, described by some as a moving form of yoga and meditation combined, evolved from martial arts and breathing exercises in China hundreds of years ago. This study uses the 24-posture standardized Tai Chi. The movements are continuous, smooth, and natural, with the upper and lower parts of the body following each other. The entire body is always in motion, with the movements performed gently and at a uniform speed. The exercise training program uses an exercise machine. The training regimen is adjusted to maintain the individual's average training heart rate at 70 to 80 percent heart rate reserve; i.e., 220 minus the person's age. Cancer survivors of solid tumor cancers who are between 18 and 65 years of age, whose treatment included chemotherapy, biologic agents or vaccines, who have had no cancer treatment for at least 24 months, and who have had no evaluable disease within 3 months of screening for this study may be eligible to participate. Participants are randomly assigned to one of three study groups: Tai Chi, exercise training, or a waiting list. Individuals in the Tai Chi and exercise training groups participate in a supervised program for 1 hour 3 times a week for 12 weeks in the NIH Clinical Center's Rehabilitation Medicine department. Individuals assigned to the waiting list are followed for 12 weeks during the waiting period and are then assigned to either the Tai Chi or exercise program for another 12 weeks as described above. At three time points during the study-before starting the program and after 6 weeks and 12 weeks of practicing the study intervention or being on the waiting list-participants undergo the following procedures: Complete questionnaires regarding their quality of life and stress Rehabilitation medicine evaluation, including the following: - Questions about managing their daily activities, whether their skills have changed over time, what they may or may not have been able to do, or what they may have had to overcome as a result of their previous illness and the study program they have been practicing - Measurements of strength and mobility - Evaluation of overall physical fitness and endurance - Blood tests to measure blood cell counts and cholesterol, lipid, hormone and mineral levels

NCT ID: NCT00094133 Recruiting - Breast Cancer Clinical Trials

Hypnosis in Treating Hot Flashes in Breast Cancer Survivors

Start date: April 2006
Phase: N/A
Study type: Interventional

RATIONALE: Hypnosis may be effective in decreasing hot flashes in breast cancer survivors. PURPOSE: This randomized clinical trial is studying how well hypnosis works in treating hot flashes in breast cancer survivors.

NCT ID: NCT00079469 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Bupropion and Counseling With or Without Contingency Management to Enhance Smoking Cessation in Treating Cancer Survivors Who Continue to Smoke

Start date: February 2004
Phase: N/A
Study type: Interventional

RATIONALE: Contingency management is a behavioral treatment approach that provides immediate rewards for positive change in behavior such as quitting smoking. In this protocol, contingency management will be in the form of a cash reward. A smoking cessation (stop-smoking) program that combines contingency management with bupropion and counseling may be effective in helping cancer survivors stop smoking. PURPOSE: Randomized clinical trial to compare the effectiveness of bupropion and counseling with or without contingency management in helping cancer survivors stop smoking.

NCT ID: NCT00075855 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Low-Dose Testosterone in Improving Libido in Postmenopausal Female Cancer Survivors

Start date: April 2004
Phase: Phase 3
Study type: Interventional

RATIONALE: The hormone testosterone may improve the libido (sex drive) in women. It is not yet known whether testosterone is effective in improving libido in female cancer survivors. PURPOSE: This randomized phase III trial is studying how well low-dose testosterone works to improve libido in postmenopausal cancer survivors.