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Behavioural Intervention
CAPABLE Intervention for Physical Disabilities (CAPABLE-VNSNY Trial)
N/A
Waitlist Available
Led By Sarah L. Szanton, PhD, RN
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Aged ≥ 65 years old
Are able to stand with or without assistance
Must not have
Do not speak English or Spanish
Have had more than 3 hospitalizations within the past 12 months
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 20-week follow-up period
Awards & highlights
No Placebo-Only Group
Summary
This trial tests the CAPABLE program, which helps older adults after hospitalization by providing home visits from a team of professionals. The goal is to improve their ability to live independently through personalized support and home modifications. The CAPABLE program aims to reduce the impact of disability among low-income older adults by addressing individual capacities and the home environment.
Who is the study for?
This trial is for older adults aged 65 or above who are part of the VNSNY CHOICE Medicare Plan, can stand (with help if needed), and have been out of the hospital for at least 60 days. They must struggle with daily tasks like walking or self-care but cannot be severely cognitively impaired, frequently hospitalized, undergoing cancer treatment, or planning to move within a year.
What is being tested?
The CAPABLE intervention is being tested to see if it helps improve sleep, balance, mobility, and self-care in older adults after they've been discharged from the hospital. It includes medication assistance, muscle and balance exercises, pain management strategies and home modifications.
What are the potential side effects?
Since CAPABLE involves non-medical interventions such as exercise and home safety improvements rather than drugs or surgery, side effects are minimal but may include muscle soreness from physical activities.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 65 years old or older.
Select...
I can stand up with or without help.
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I struggle with daily self-care activities.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not speak English or Spanish.
Select...
I have been hospitalized more than 3 times in the last year.
Select...
I am currently undergoing radiation or chemotherapy.
Select...
I have been diagnosed with a serious brain condition that could be fatal within a year.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 20-week follow-up period
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~20-week follow-up period
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Mean ADL Difficulty Score
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
The experimental group will receive CAPABLE services. These include ≤10 sessions: ≤ 6 with an Occupational Therapist (OT) and ≤ 4 sessions with a Registered Nurse (RN) and up to ≤ $1,500 of home safety and home modifications from a licensed handyman who is guided by the OT. The OT and RN sessions will target participants' self-identified functional goals (e.g., getting safely into the tub, getting upstairs to sleep in own bed).
Group II: Usual CareActive Control1 Intervention
Participants in the usual care group will not receive visit from study clinicians and will continue to receive their usual VNSNY CHOICE benefits and healthcare.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for physical disabilities, particularly those involving integrated health services like comprehensive rehabilitation and support, work through several mechanisms. Physical therapy and exercise programs focus on muscle strengthening and balance training, which improve mobility and prevent falls.
Pain management techniques reduce discomfort, allowing for more active participation in daily activities. Home modifications create safer environments, reducing the risk of injury.
These interventions are essential for patients with physical disabilities as they collectively enhance independence, improve quality of life, and minimize the risk of further disability.
A COMBINED TREATMENT APPROACH EMPHASIZING IMPAIRMENT-BASED MANUAL THERAPY AND EXERCISE FOR HIP-RELATED COMPENSATORY INJURY IN ELITE ATHLETES: A CASE SERIES.Multidisciplinary rehabilitation after primary brain tumour treatment.Evidence-based analysis of physical therapy in Parkinson's disease with recommendations for practice and research.
A COMBINED TREATMENT APPROACH EMPHASIZING IMPAIRMENT-BASED MANUAL THERAPY AND EXERCISE FOR HIP-RELATED COMPENSATORY INJURY IN ELITE ATHLETES: A CASE SERIES.Multidisciplinary rehabilitation after primary brain tumour treatment.Evidence-based analysis of physical therapy in Parkinson's disease with recommendations for practice and research.
Find a Location
Who is running the clinical trial?
Johns Hopkins UniversityLead Sponsor
2,321 Previous Clinical Trials
14,873,673 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,782 Previous Clinical Trials
28,183,825 Total Patients Enrolled
Sarah L. Szanton, PhD, RNPrincipal InvestigatorJohns Hopkins University
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not speak English or Spanish.I have been hospitalized more than 3 times in the last year.I am 65 years old or older.I am currently undergoing radiation or chemotherapy.I can stand up with or without help.I have been diagnosed with a serious brain condition that could be fatal within a year.I struggle with daily self-care activities.
Research Study Groups:
This trial has the following groups:- Group 1: Intervention
- Group 2: Usual Care
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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