N/A
N=50
Aging With Long Term Physical Disabilities
Physical Disability
Bottom Line
View on ClinicalTrials.gov: NCT04589988 ↗Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcome: Primary: In-Home Occupational Performance Evaluation (I-HOPE) Activity Score — 0.73; 0.72; 0.76; 0.69 score on a scale — p=0.068
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Removing Environmental Barriers to Independent Living (REBIL) (Behavioral); Waitlist Attentional Control (Behavioral)
- Age
- Adult, Older Adult · 45+ yrs
- Sex
- All
- Sponsor
- Washington University School of Medicine
- Primary completion
- Jun 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY In-Home Occupational Performance Evaluation (I-HOPE) Activity Score |
0.73; 0.72; 0.76; 0.69 | 0.068 |
| PRIMARY In-Home Occupational Performance Evaluation (I-HOPE) Performance Score |
2.49; 2.52; 3.23; 2.87 | 0.063 |
| PRIMARY In-Home Occupational Performance Evaluation (I-HOPE) Satisfaction Score |
2.12; 2.09; 2.86; 2.74 | 0.724 |
| PRIMARY In-Home Occupational Performance Evaluation (I-HOPE) Barrier Severity Score |
50.28; 51.83; 21.93; 27.79 | 0.447 |
| PRIMARY Reintegration to Normal Living Index (RNLI) |
65.59; 66.10; 70.08; 68.90 | 0.696 |
| PRIMARY Westmead Home Safety Assessment (WeHSA) Short Form |
10.52; 9.94; 7.04; 6.94 | 0.798 |
| SECONDARY Fall Prevention Strategy Survey (FPSS) |
13.2; 13.9; 16.5; 15.2 | 0.135 |
| SECONDARY Participation Scale |
0.54; 0.58; 0.65; 0.63 | 0.291 |
| SECONDARY Fall Rate |
15; 17.6 | 0.631 |
Summary
The purpose of this study is to determine the feasibility and efficacy of an adapted evidence-based program (REBIL) to reduce barriers to community participation and remove fall hazards at home for adults aging with physical disabilities.
Eligibility Criteria
Inclusion Criteria
- Age 45-65 years
- Self-report of difficulty with at least 2 daily activities using the Older Adult Retirement Survey Activities of Daily Living (OARS ADL) scale
- onset of a physical disability 5 years prior to participation (e.g., spinal cord injury (SCI), cerebral palsy, post-polio syndrome, stroke, amputation).
- live within 60 miles of the research lab
Exclusion Criteria
- Currently institutionalized.
Data sourced from ClinicalTrials.gov (NCT04589988). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.