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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02090192
Other study ID # ChinaPLAGH-2013FC3009
Secondary ID
Status Recruiting
Phase N/A
First received March 14, 2014
Last updated March 16, 2014
Start date January 2013
Est. completion date December 2015

Study information

Verified date March 2014
Source Chinese PLA General Hospital
Contact Li Zhang, Doctor
Phone 8610-66876335
Email zhangli781230@163.com
Is FDA regulated No
Health authority China: Ethics CommitteeChina: Ministry of Health
Study type Interventional

Clinical Trial Summary

Objective: To study the acute and chronic effects of whole-body vibration (WBV) exercises on the lower extremity blood flow, mobility function, balance, muscle strength, bone density, and general health status, and its feasibility as an intervention in frail elderly patients.

Design: Randomized controlled trial. Subjects: The frail older persons meeting the Fried Frailty Criteria.

Interventions: All eligible subjects were randomly assigned to 4 groups:

(1) WBV group: Subjects received a whole-body vibration exercise alone; (2) Progressive resistance training (PRT) group: Subjects received progressive resistance training; (3) WBV+ PRT group: Subjects received the whole-body vibration and progressive resistance training; (4) Control group: Subjects received no intervention/training. The periods of intervention are 12 weeks.

Main measures: The lower extremities blood flow (the diameters and red blood cell velocity of the common femoral artery), timed up and go test, 30-second chair stand test, five times sit to stand test, lower extremities muscle strength, balance function, balance confidence, bone density, and general health status was assessed at the beginning of the study, at instant, 12 weeks and 24 month after the intervention.

Study hypothesis: Whole-body vibration exercise is a safe and effective method that can improve the lower extremity blood flow, mobility function, balance, muscle strength, bone density, and general health status in the frail elderly.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 75 Years and older
Eligibility Inclusion Criteria:

- =75 years old

- Fried Frailty Criteria

- Mini Mental State Examination score =18

Exclusion Criteria:

- Recent fractures (=6 months)

- Gallbladder or kidney stones

- Malignancies

- Rheumatic arthritis

- Epilepsy

- Serious heart sicknesses or an implant, and bypass stent or cardiac pacemaker

- Any diseases to be associated with a life expectancy of less than 12 months

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
WBV training

PRT training


Locations

Country Name City State
China Rehabilitation Department, Nanlou, Chinese PLA general hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Li Zhang

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of the common femoral artery's blood flow from Baseline to 60min post-WBV 60min post-WBV No
Primary Change of lower extremities muscle strength from Baseline to 3 month post-WBV 3 month post-WBV No
Primary Change of "timed up and go" test (TUGT) from Baseline to 3 month post-WBV 3 month post-WBV No
Primary Change of 30-second chair stand test from Baseline to 3 month post-WBV 3 month post-WBV No
Primary Change of balance function from Baseline to 3 month post-WBV 3 month post-WBV No
Primary Change of balance confidence from Baseline to 3 month post-WBV 3 month post-WBV No
Primary Change of bone density from Baseline to 6 month post-WBV 6 month post-WBV Yes
Primary Change of general health status (SF-12 score) from Baseline to 6 month post-WBV 6 month post-WBV No
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