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Implementing Resistance Exercise to Reduce Frailty for Older Adult

Implementing Resistance Exercise to Reduce Frailty for Older Adult Medicaid Waiver Recipients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02942992
Enrollment
126
Registered
2016-10-24
Start date
2017-03-30
Completion date
2018-07-31
Last updated
2019-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Brief summary

To develop an intervention specifically targeted for these clients who have the frailty syndrome. The Investigators propose to develop an exercise intervention that can reduce frailty in older adults to facilitate their ability to age-in-place. The long-term objective of this work is to develop a package of interventions that can be administered within the existing Medicaid Home and Community Based Services (HCBS) Waiver programs. The specific goal of this proposal is to develop a resistance exercise intervention to reduce frailty in older adults receiving long term care services in their home through the Illinois Community Care Program, a HCBS Waiver Program.

Interventions

BEHAVIORALResistance exercise

resistance exercise

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

for Home Care Aides: \- Employees of Help at Home, with one eligible client Inclusion criteria for clients: * aged 65+ years * receive HCA services two or more days per week * English-speaking * not currently participating in regular exercise as defined as 30 minutes three or more days per week, - - no health problems that contraindicate participation in exercise based on the EASY: Exercise Assessment and Screening for You * Telephone Interview for Cognitive Status score \> 26

Exclusion criteria

for HCAs: \- no clients who enroll in the study

Design outcomes

Primary

MeasureTime frame
Number of participants with frailty or pre-frailty as assessed by the SHARE-FI26 weeks

Secondary

MeasureTime frame
Scores of self-reported overall health as measured by the PROMIS-global health26 weeks
Quadriceps muscle strength as assessed by the 30 second chair rise test26 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026