Power Centering for Seniors

Last updated on July 2021

Recruitment

Recruitment Status: Recruiting
Estimated Enrollment: Same as current

Summary

Conditions

Healthy Aging
Mobility Limitation
Walking, Difficulty

Type

Interventional

Phase

Not Applicable

Design

Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: This delayed intervention trial begins as a parallel group design with the Delayed Intervention (Dl) group serving as a control arm comparison for the Immediate Intervention (II) group. There is no control intervention. The ll and the Dl groups will be assessed pre-intervention. After the 12-week intervention for the II group, resp. the waiting period for the DI group, the lI group will undergo their post-intervention assessment. At that time, the Dl group will undergo their 2nd pre-intervention assessment to document any change in baseline measures that may have occurred. No significant changes are expected, so that at the end of the trial, data from the ll and the Dl groups can be pooled to provide results on the overall changes in outcome measures for all participants post- versus pre-intervention. After the 2nd pre-intervention assessment, the Dl group will have their intervention, post-intervention assessment, follow-up period and final assessment, as with the II group.Masking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age: Between 70 years and 125 years
Gender: Both males and females

Description

Not Provided

Tracking Information

NCT #: NCT04861831
Collaborators: Not Provided
Investigators: Principal Investigator: Stephanie A. Bridenbaugh, M.D. University Department of Geriatric Medicine FELIX PLATTER