Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00421057 · ClinicalTrials.gov registry record
Combined Strength Training and Functional Endurance Exercise Regimen on Cancer -Related Fatigue and Physical Performance
A clinical trial, sponsored by M.D. Anderson Cancer Center.
- Completed
- Registry status
- 25
- Enrollment target
NCT00421057: Completed study, sponsored by M.D. Anderson Cancer Center.
NCT00421057 is a clinical trial that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 25 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00421057 has completed, sponsored by M.D. Anderson Cancer Center.
- COMPLETED
- Registry status
- 25 participants
- Enrollment target
Study Summary
Primary Objective: -Determine if a specific exercise regimen (combined strength training/functional endurance) reduces the level of fatigue among women with breast cancer while undergoing adjuvant or neoadjuvant chemotherapy treatment as compared to a control group. Secondary Objectives: * Determine if a specific exercise regimen (combined strength training/functional endurance) increases the overall ability to perform daily physical activities (ADLs) among women with breast cancer while undergoing adjuvant or neoadjuvant chemotherapy treatment as compared to a control group. * Determine if a specific exercise regimen (combined strength training/ functional endurance) increases mobility in women with breast cancer while undergoing adjuvant or neoadjuvant chemotherapy treatment as compared to a control group. * Determine if a specific exercise regimen (combined strength training/functional endurance) increases endurance in women with breast cancer while undergoing adjuvant or neoadjuvant chemotherapy as compared to a control group.
Primary Outcome
Self-reported score that measures subjective perceptions of fatigue in which respondents rate their experience of feeling tired. It ranges from 1 (not at all) to 5 (extremely) and describes discomforts of cancer related fatigue in four dimensions (physical, mental, emotional, and temporal) (Schwartz and Meek, 1999).
Interventions
- BEHAVIORAL Questionnaire
- BEHAVIORAL Combined Strength Training and Functional Endurance Exercise
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2007-01 |
| Est. Completion | 2009-03 |
What the finished NCT00421057 record still lists
NCT00421057 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 25 participants, a relatively small participant target.
The record links to 0 conditions, and to 2 interventions - of which Questionnaire is the first listed.
NCT00421057 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00421057 about?
NCT00421057 is a clinical study titled "Combined Strength Training and Functional Endurance Exercise Regimen on Cancer -Related Fatigue and Physical Performance". Primary Objective: -Determine if a specific exercise regimen (combined strength training/functional endurance) reduces the level of fatigue among women with breast cancer while undergoing adjuvant or neoadjuvant chemotherapy treatment as compared to a control group. Secondary Objectives: * Determ...
What is the current status of trial NCT00421057?
This trial is currently completed. The enrollment target is 25 participants. The study started on 2007-01. Estimated completion is 2009-03.
What interventions are being tested in trial NCT00421057?
The interventions under investigation include: Questionnaire (BEHAVIORAL), Combined Strength Training and Functional Endurance Exercise (BEHAVIORAL).
Who is sponsoring clinical trial NCT00421057?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01166854 · 25 participants
Characterization of Familial Myopathy and Paget Disease of Bone
- NCT01913106 · 25 participants · Phase 1
HSV-tk + Valacyclovir Therapy in Combination With Brachytherapy for Recurrent Prostate Cancer
- NCT02138669 · 25 participants · NA
Intacs Prescription Inserts for Keratoconus Patients
- NCT02174549 · 25 participants · Phase 1
Dose-defining Study of Tirapazamine Combined With Embolization in Liver Cancer
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia