Effect of Tai Chi Vs. Structured Exercise on Physical Fitness and Stress in Cancer Survivors
NCT ID: NCT00246818
Last Updated: 2017-07-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
76 participants
INTERVENTIONAL
2005-10-26
2011-02-25
Brief Summary
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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
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Detailed Description
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This study aims to compare in a randomized, wait-list controlled design, the efficacy of TCC to an exercise program in improving aerobic exercise capacity and endurance, reducing stress and improving Quality of Life in adult survivors of malignant solid tumors.
Conditions
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Study Design
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TREATMENT
Interventions
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Tai Chi Chuan
Eligibility Criteria
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Inclusion Criteria
Diagnosis of solid cancer
Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 1
Age 18 - 65 years at time of study enrollment
Patients must be considered cancer survivors defined either as:
In the first continued remission from cancer after completion of initial therapy (i.e., No Evaluable Disease (NED) for greater than 2 years after successful completion of initial cancer therapy) or
In continued remission for greater than 5 years after completion of salvage therapy for disease recurrence
Must have completed cancer treatment regimen that includes chemotherapy, biologic agents (e.g. IL-2, interferon) or vaccines
Patients must have had no cancer treatment (e.g., chemotherapy, radiation therapy, cancer related surgery and/or immunotherapy) within the last 24 months
Patients must be free of recurrence at the time of evaluation (e.g., No Evaluable Disease (NED) by history and evaluation within the past 3 months)
Must be able to understand and sign consent.
Exclusion Criteria
History of CAD/Angina or cardiomyopathy
History of CVA/stroke
Current clinical diagnosis of major depression
Prior or current practice of Tai Chi Chuan
Inability to perform and follow study intervention routine or study assessments/measures according to assessment of Principal Investigator, Rehabilitation Medicine Physician or TCC instructor (Dr. Adeline Ge).
Treatment with stimulants, antidepressants (for diagnosis of major depression), neuroleptics, betablockers or cardiac antiarrhythmics.
Current enrollment on or participation in a regular, structured exercise program.
18 Years
65 Years
ALL
No
Sponsors
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National Center for Complementary and Integrative Health (NCCIH)
NIH
Locations
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National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States
Countries
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References
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Chernecky C. Temporal differences in coping, mood, and stress with chemotherapy. Cancer Nurs. 1999 Aug;22(4):266-76. doi: 10.1097/00002820-199908000-00003.
Hughes J. Emotional reactions to the diagnosis and treatment of early breast cancer. J Psychosom Res. 1982;26(2):277-83. doi: 10.1016/0022-3999(82)90047-2.
Sabbioni ME, Bovbjerg DH, Jacobsen PB, Manne SL, Redd WH. Treatment related psychological distress during adjuvant chemotherapy as a conditioned response. Ann Oncol. 1992 May;3(5):393-8. doi: 10.1093/oxfordjournals.annonc.a058214.
Other Identifiers
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06-AT-0016
Identifier Type: -
Identifier Source: secondary_id
060016
Identifier Type: -
Identifier Source: org_study_id
NCT00414791
Identifier Type: -
Identifier Source: nct_alias
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