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Influence of Exercise on Anemia in MDS Patients

This study has been withdrawn prior to enrollment.
(We were unable to find patients that fit the eligibility criteria.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01783249
First Posted: February 4, 2013
Last Update Posted: February 4, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University of Rochester
  Purpose
That exercise will reduce anemia and fatigue, while improving aerobic capacity, strength and hematopoietic stem and progenitor cell mitochondrial function.

Condition Intervention Phase
Feasibility Pilot Study Other: Stationary Exercise cycling Phase 1 Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: The Influence of Exercise on Anemia in MDS Patients

Resource links provided by NLM:


Further study details as provided by University of Rochester:

Primary Outcome Measures:
  • Feasibility data on the effect of a stationary cycling program
    Aim to provide preliminary feasibility data on the effect of a stationary cycling program on anemia and acrocytosis, fatigue, aerobic capacity, strength, and hematopoietic stem and progenitor cell mitochondrial function in MDS patients.


Enrollment: 0
Study Start Date: November 2011
Study Completion Date: November 2012
Estimated Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
No Intervention: Control
Usual care monitoring
Exercise using stationary cycling
Stationary cycling exercise program
Other: Stationary Exercise cycling
Stationary exercise cycling

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:Have a confirmed diagnosis of MDS, Have approval of the study medical monitor, be able to read English, be 21 years of age or older, give informed consent -

Exclusion Criteria: Have physical limitations, be identified in the active or maintenance stage of exercise behavior

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01783249


Locations
United States, New York
James P. Wilmot Cancer Center, University of Rochester
Rochester, New York, United States, 14642
Sponsors and Collaborators
University of Rochester
  More Information

Responsible Party: University of Rochester
ClinicalTrials.gov Identifier: NCT01783249     History of Changes
Other Study ID Numbers: 37173MDS
First Submitted: November 30, 2011
First Posted: February 4, 2013
Last Update Posted: February 4, 2013
Last Verified: January 2013