Fall Recovery Training for Older Adults in Continuous Care Facilities
Tab Title Description
Describes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
- Rochester, Minnesota: 13-000605
NCT ID: NCT02173015
Sponsor Protocol Number: 13-000605
About this study
The purpose of this study is to evaluate the effect that a new fall prevention training program has on the fall incidence of long-term care facility residents at high-risk of falling.
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
- Subjects must be 50 years or older, living in continuous-care retirement facilities.
- For participation in study:
- Three or more errors on the Six-Item Screener for Cognitive Impairment
- Individuals who cannot provide consent for themselves
- For participation in compensatory step training:
- Physician or nurse practitioner approval to participate in the study with the guidelines that subjects should not participate if any of the following is applicable:
- Unable to walk one block without stopping or using a walking aid (self-reported)
- Acute illness at the time of functional assessment or training
- Body mass greater than 114 kg
- Body size too large for wearing a safety harness
- Lower extremity joint replacement within a year prior to participation
- Femoral neck or total hip bone mineral density t-score less than -2.5
- Based on a dual-energy X-ray absorptiometry (DXA) scan in the Mayo Clinic Charlton Clinical Research Unit (CRU), with no medication changes that may affect bone mineral density at the hip (e.g. starting prednisone). During the visit to the CRU, the subject's height and weight will be measured.
- If the subject has had a hip DXA scan within 6 months of participation, the exclusion criterion will be based on the previous scan.
- If the subject has had bilateral hip replacement, then the subject will not qualify for compensatory step training.
- Parkinson's disease
- A history of stroke
- A history of back surgery
- Bulging vertebral discs
- Spine, hip, or lower extremity fracture within a year prior to participation
- Open lesions on the lower extremity
- In case of lower extremity amputation, stump volume fluctuations within a year of training
- Use of a pacemaker
- Use of an ostomy pouch
- Doctor recommendation to avoid moderate physical activity or exercise
- Any neural, muscular, or skeletal condition or injury that precludes safe participation in the training, at the discretion of the clinician or study staff.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
|Mayo Clinic Location
Mayo Clinic principal investigator
Kenton Kaufman, Ph.D.
Closed for enrollment
Publications are currently not available