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CAPABLE for Frail Dually Eligible Older Adults

CAPABLE for Frail Dually Eligible Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01743495
Acronym
CAPABLE500
Enrollment
281
Registered
2012-12-06
Start date
2012-09-30
Completion date
2019-08-31
Last updated
2020-02-12

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

Conditions

Muscle Weakness

Keywords

Medical Costs, improved IADLs, and/or ADL's, decreased nursing home admissions

Brief summary

The Johns Hopkins School of Nursing offers this research study which aims to learn more about whether services that help with medications, muscle strengthening, pain management and changes to houses can help improve older adults' ability to, walk, and take care of themselves while saving costs by reducing hospitalizations and nursing home admissions.

Detailed description

* 65yrs or older * Be able to stand (with or without assistance) * Have some difficulty with getting dressed, or preparing food, bathing * Receive a low monthly income * Have no plans to move in the next year * NOT be receiving home nursing or other therapy right now

Interventions

BEHAVIORAL10 home-based functional services sessions over 4 months.

The program consists of up to 10 home-based functional services sessions over 4 months.

Sponsors

Centers for Medicare and Medicaid Services
CollaboratorFED
Baltimore City Health Department
CollaboratorOTHER
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* 65 or older * Cognitively intact (≥ 10 on Brief Interview of Mental Status) * Difficulty with ≥ 2 IADLS or ≥ 1 ADL * ≤ 199% of Federal Poverty level

Exclusion criteria

* Terminally ill --Active cancer treatment * Hospitalized \> 3 times in last 3 years * Receiving home nursing, Occupational Therapy or Physical Therapy * Don't have phone or do plan to move in less than a year

Design outcomes

Primary

MeasureTime frameDescription
Cost Effectiveone year after interventionChart review to see change between cost of intervention to medicaid before and after CAPABALE

Secondary

MeasureTime frameDescription
Quality of Life as assessed by the Activities of Daily Living (ADL) Questionnairefour months post interventionThe ADL Questionnaire will be used to assess quality of life in participants. The score ranges from 0 to 32, with 0 being no help required with activities of daily life and 32 representing that the participant is incapable of completing activities of daily life regardless of difficulty without assistance.
Quality of Life as assessed by the ADL Questionnaireeight months post interventionThe ADL Questionnaire will be used to assess quality of life in participants. The score ranges from 0 to 32, with 0 being no help required with activities of daily life and 32 representing that the participant is incapable of completing activities of daily life regardless of difficulty without assistance.
Quality of Life as assessed by the Instrumental Activities of Daily Living (IADL) Questionnairefour months post interventionThe IADL Questionnaire will be used to assess quality of life in participants. The score ranges from 0 to 32, with 0 being no help required with activities of daily life and 32 representing that the participant is incapable of completing instrumental activities of daily life regardless of difficulty without assistance.
Quality of Life as assessed by the IADL Questionnaireeight months post interventionThe IADL Questionnaire will be used to assess quality of life in participants. The score ranges from 0 to 32, with 0 being no help required with activities of daily life and 32 representing that the participant is incapable of completing instrumental activities of daily life regardless of difficulty without assistance.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026