Randomized ActiveStep Clinical Evaluation (RACE)
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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. |
| ClinicalTrials.gov Identifier: NCT00810082 |
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Recruitment Status :
Completed
First Posted : December 17, 2008
Results First Posted : March 26, 2012
Last Update Posted : May 23, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Fall Prevention | Device: ActiveStep Other: Standard Physical Therapy for Fall Prevention | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 65 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Prevention |
| Official Title: | Randomized ActiveStep Clinical Evaluation |
| Study Start Date : | December 2008 |
| Actual Primary Completion Date : | December 2009 |
| Actual Study Completion Date : | December 2009 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: Group A
Standard physical therapy for fall prevention
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Other: Standard Physical Therapy for Fall Prevention
Standard physical therapy for fall prevention |
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Experimental: Group B
Physical therapy for fall prevention that includes ActiveStep
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Device: ActiveStep
ActiveStep™ is a training simulator. The system uses a computer-controlled treadmill to recreate life-like dynamic balance challenges such as slipping and tripping in a safe, controlled environment. Other: Standard Physical Therapy for Fall Prevention Standard physical therapy for fall prevention |
- Participants With at Least One Fall [ Time Frame: 3 months ]Subjects who had at least one fall subsequent to treatment.
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| Ages Eligible for Study: | 65 Years and older (Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age 65 or older
- Referred for balance training
Exclusion Criteria:
- Age < 65
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): NCT00810082
| United States, New Hampshire | |
| Dartmouth-Hitchcock Medical Center | |
| Lebanon, New Hampshire, United States, 03756 | |
| Alice Peck Day Memorial Hospital | |
| Lebanon, New Hampshire, United States, 03766 | |
| Principal Investigator: | Jon D Lurie, MD, MS | Dartmouth College | |
| Principal Investigator: | Richard M Greenwald, PhD | Simbex Corporation |
| Responsible Party: | Dartmouth-Hitchcock Medical Center |
| ClinicalTrials.gov Identifier: | NCT00810082 |
| Other Study ID Numbers: |
TDI001 |
| First Posted: | December 17, 2008 Key Record Dates |
| Results First Posted: | March 26, 2012 |
| Last Update Posted: | May 23, 2018 |
| Last Verified: | April 2018 |

