Neurophysiological Evaluation of Training Effect on Cancer-Related Weakness
| Status: | Recruiting |
|---|---|
| Conditions: | Breast Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 40 - 75 |
| Updated: | 1/21/2018 |
| Start Date: | May 2016 |
| End Date: | September 2019 |
| Contact: | Didier Allexandre, PhD |
| Email: | dallexandre@kesslerfoundation.org |
| Phone: | 9733243525 |
Breast cancer patients often suffer from long-term physical symptoms of weakness. In this
study, investigators propose to compare how two different low intensity physical exercise
training programs can improve handgrip strength for breast cancer patients with symptoms of
weakness. Using brain imaging, the study will also investigate changes in brain structure,
and muscle activity associated with handgrip.
study, investigators propose to compare how two different low intensity physical exercise
training programs can improve handgrip strength for breast cancer patients with symptoms of
weakness. Using brain imaging, the study will also investigate changes in brain structure,
and muscle activity associated with handgrip.
Participants will be randomized to either a no treatment group or one of two low intensity
6-week exercise training. Outcomes will be measured at baseline, post-intervention and 4
weeks post intervention.
6-week exercise training. Outcomes will be measured at baseline, post-intervention and 4
weeks post intervention.
Inclusion Criteria:
- Female aged 40-75 yrs
- Right handed, as determined by the Edinburgh Inventory (Oldfield, 1971)
- Proficient in English
- Must be available for the familiarization, and testing sessions
Exclusion Criteria:
- Symptoms for mild or severe depression as determined by a Patient Health Questionnaire
(PHQ-8) score >14
- Significant cognitive impairments as defined by a score <28 in the Folstein
Mini-Mental Screening Examination (MMSE, Folstein et al .1975).
- Participated in any type of motor imagery or strength training program in the last 5
years, or plan to start any motor imagery or physical strength training program for
the 3 months duration of the study
- Neurological, psychiatric, musculoskeletal or other types of disorder that may affect
participants sensorimotor function and cognitive abilities
- Current medication believed to affect cognitive/psychomotor function (i.e., opioid,
analgesics, anxiolytics or antidepressants)
- History of alcohol, smoking, and drug abuse
- Any contraindication for MRI
We found this trial at
2
sites
West Orange, New Jersey 07052
Principal Investigator: Michael Stubblefield, PhD
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West Orange, New Jersey 07052
Principal Investigator: Guang Yue, PhD
Phone: 973-324-3525
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