- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03252262
Power V360 - Promoting Optimal Wellness Among Elders Through Vitalize 360
August 14, 2017 updated by: Hebrew SeniorLife
The primary purpose of this project was to implement Vitalize 360, a comprehensive assessment system and wellness coaching program for vulnerable, low income, community dwelling older adults, and to determine if this program is effective in promoting and sustaining self-management skills to increase well-being and functional health among this group.
Designed specifically for community-dwelling older adults, Vitalize 360 provides a unique opportunity to guide elders in selecting personal goals that align with their assessment results and develop an action plan for goal achievement.
This strategy holds potential as an effective mechanism to empower elders to implement behaviors that promote healthy aging.
Study Overview
Detailed Description
The purpose of this project was to determine if Vitalize 360, a comprehensive assessment system and wellness coaching program was effective in promoting and sustaining increased physical activity and improved mood, health status and quality of life.
A repeated measures, secondary analysis design was the selected approach Data from 161 participants were used to test the hypotheses.
After one year, the sample had improvement with increased socialization while physical activity level fluctuated over time suggestive of a seasonality effect.
Paired t-tests and repeated measures analysis revealed no statistically significant improvement in physical activity level, mood, health status or quality of life.
Vitalize 360 provides a unique opportunity to guide elders in selecting personal goals that align with their assessment results and develop an action plan for goal achievement.
When used among vulnerable and frail elders, some modifications are needed to provide sustained, favorable outcomes.
Study Type
Interventional
Enrollment (Actual)
161
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
58 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
Age 60 years and over, residing in subsidized housing sites operated by Hebrew SeniorLife and participating in Vitalize 360 program
Exclusion Criteria:
younger than 60 years, not participating in Vitalize 360 program and not a permanent resident of housing sites.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Jack Satter House
Residents of Jack Satter House who participated in the Vitalize 360 Program.
|
A comprehensive geriatric assessment system and wellness coaching program.
|
Active Comparator: Center Communities of Brookline
Residents of Center Communities of Brookline who participated in the Vitalize 360 Program.
|
A comprehensive geriatric assessment system and wellness coaching program.
|
Active Comparator: Simon C. Fireman
Residents of Simon C. Fireman who participated in the Vitalize 360 Program
|
A comprehensive geriatric assessment system and wellness coaching program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical Activity Level
Time Frame: 18 months
|
number of hours engaged in physical activity over the past 3 days
|
18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Elizabeth P Howard, PhD, Hebrew Rehabilitation Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 30, 2014
Primary Completion (Actual)
December 30, 2015
Study Completion (Actual)
December 30, 2015
Study Registration Dates
First Submitted
April 12, 2017
First Submitted That Met QC Criteria
August 14, 2017
First Posted (Actual)
August 17, 2017
Study Record Updates
Last Update Posted (Actual)
August 17, 2017
Last Update Submitted That Met QC Criteria
August 14, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- P 30 AG048785
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
Contact PI to obtain approval for use of COLLAGE/interRAI data
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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