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Sponsored by: |
M.D. Anderson Cancer Center |
Information provided by: | M.D. Anderson Cancer Center |
ClinicalTrials.gov Identifier: | NCT00601133 |
Primary Objective:
1. To determine the change in functional tests of postural control of cancer patients who have completed acute inpatient rehabilitation from discharge at one month (+/-1wk) after discharge.
Secondary Objective:
1. To assess the correlations between the functional tests of postural control, the balance test and the amount of exercise per week.
Condition | Intervention |
Solid Tumors |
Other: Walking Test Other: Balance Test Behavioral: Questionnaire Behavioral: Diary |
MedlinePlus related topics: | Cancer Exercise and Physical Fitness Rehabilitation |
Drug Information available for: | Benzocaine |
Study Type: | Observational |
Study Design: | Case-Only, Prospective |
Official Title: | Quantitative and Clinical Description of Postural Instability in Patient Who Underwent Acute Inpatient Rehabilitation and at Follow-Up |
Estimated Enrollment: | 58 |
Study Start Date: | January 2008 |
Estimated Primary Completion Date: | January 2009 (Final data collection date for primary outcome measure) |
Groups/Cohorts | Assigned Interventions |
1
Participants having difficulty walking and with balance after cancer treatment that are leaving the M.D. Anderson rehabilitation hospital.
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Other: Walking Test
Timed Test 1: From sitting position walk 10 feet quickly, return to sitting position Timed Test 2: Walk 25 feet, turn around, and walk back Tests conducted twice, once on departure from rehabilitation center, and again at a return visit 1 month later
Machine balance test: Stand on a platform with a rail, shift weight and try to maintain balance and center of gravity; Results displayed.
Behavioral: Questionnaire
To be completed when leaving the rehabilitation program and again at the study visit 1 month later, lasting about 5 minutes.
Behavioral: Diary
Record any physical exercise done from departure of rehabilitation center to return visit 1 month later; includes exercises; approximately 5 minutes per entry
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To be enrolled in this study, you must be able to walk with or without an assistant device (such as a cane or a walker).
STUDY PROCEDURES:
If you are found to be eligible to take part in this study, you will do a combination of walking and balance tests twice, once on the day you leave the rehabilitation center, and again at a return visit 1 month later. For the first test, you will get up from a chair and walk 10 feet as quickly, but as safely, as possible. You will then return to the chair and sit again. For the second test, you will walk 25 feet, turn around, and walk back to the starting point as fast and as safely as you can. Both tests will be timed by the study staff.
You will also do a balance test on a machine. You will stand on a platform with a rail to hold on to. You will shift your weight and try to keep your balance and center of gravity, which will be shown on a screen.
You will be given a diary to record any physical exercise you are doing from the time you leave the rehabilitation center to your return visit 1 month later. You will be asked to record what kind of exercises (home exercise, home health therapy, or outpatient therapy treatment) you do and for how many hours. It should take about 5 minutes to fill out the diary each time.
You will complete a questionnaire that asks you about your symptoms, such as pain. You will complete it when you leave the rehabilitation program and again at the study visit 1 month later. It should take about 5 minutes to complete the questionnaire.
LENGTH OF STUDY:
You will be off study after you complete the second questionnaire.
This is an investigational study. Up to 58 patients will take part in this study. All will be enrolled at M. D. Anderson.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Patients who have completed acute inpatient rehabilitation at MDACC
Inclusion Criteria:
Exclusion Criteria:
Contact: Ying Guo, MD | 713-745-2327 |
United States, Texas | |||||
U.T.M.D. Anderson Cancer Center | Recruiting | ||||
Houston, Texas, United States, 77030 | |||||
Principal Investigator: Ying Guo, MD |
M.D. Anderson Cancer Center |
Principal Investigator: | Ying Guo, MD | U.T.M.D. Anderson Cancer Center |
The University of Texas M.D.Anderson Cancer Center 
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Responsible Party: | U.T.M.D. Anderson Cancer Center ( Ying Guo, MD/Associate Professor ) |
Study ID Numbers: | 2007-0799 |
First Received: | January 14, 2008 |
Last Updated: | October 3, 2008 |
ClinicalTrials.gov Identifier: | NCT00601133 |
Health Authority: | United States: Institutional Review Board |
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