Supplemental Mobility
Part of paid clinical trials in Aurora, Colorado.
- Sponsor
- University of Colorado, Denver
- Study ID
- NCT07872384
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Aging
- Deconditioning
- Functional Recovery
- Medically Complex
- Skilled Nursing Facility
Eligibility Criteria
- Sex
- ALL
- Age
- 50 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- High Intensity Rehabilitation — OTHERAn 8RM is the dose necessary for most effective strength gains in community-dwelling older adults, and is equivalent to 80% of a one repetition max, which is the maximal load needed to voluntarily complete one repetition of a given exercise with proper form. Activities will include strength training, transfer practice, balance training, advanced ADLs. Clinicians will tailor the intervention for each activity to target overload using 8-repetition maximum for resistance training. Other interventions will be performed to muscle failure or inability to complete the final repetition. Failure is the inability to complete a repetition through the full, available range of motion without significant compensation. Further, high-intensity dosing requires continuous, volitional effort from the patient; therefore, incorporation of motivational interviewing strategies across sessions will maximize patient effort and self-efficacy.
- Safe Transfers and Mobility Program — OTHERThe Safe Transfers and Mobility Program (STAMP) embeds a mobility aide into daily care. STAMP is a patient-centered, scalable approach to extend the benefits of rehabilitation sessions by increasing mobility throughout the day and reinforcing activity between therapy sessions. Core components are: (1) targeting 45 minutes of additional daily physical activity through support with walking and functional mobility tasks; (2) establishing individualized mobility goals collaboratively set by the therapist and patient, based on functional level; (3) delivering progressive activities with walking distances increased by \~30% weekly, adjusted for patient tolerance; and (4) interdisciplinary coordination to incorporate STAMP sessions into routine care with minimal disruption to clinical workflow. Prior work suggests that 45 minutes of STAMP can at least double daily step counts, and increasing walking distance by 30% per week is feasible even for individuals with low baseline function.
- Usual Care — OTHERUsual Care SNFs will continue with routine collection and documentation of physical performance outcomes (gait speed, SPPB, Modified Barthel ADL Index) as standard practice. Importantly, the Usual Care SNF including the facility, rehabilitation clinicians, and patients will not have access to i-STRONGER materials.
Study Details
This pilot study will evaluate the feasibility of a supplemental mobility intervention, the Safe Transfers And Mobility Program (STAMP). This program will be implemented in patients admitted to skilled nursing facilities (SNFs) following hospitalization. STAMP will be administered by a mobility aide who will support patients in increasing physical activity through walking and transfers outside of structured rehabilitation. Participants will either receive high-intensity rehabilitation (HIR) or usual care rehabilitation, combined with STAMP. The two main aims are: 1) determine the feasibility, acceptability, and safety of STAMP, and 2) evaluate the feasibility and variability of patient physical function outcome measures. The study will provide preliminary data on program delivery and safety to inform the design of a larger trial aimed at identifying the most effective strategies to optimize functional recovery in SNFs.
Key Dates
- First listed
- Oct 13, 2026
- Start date
- Sep 30, 2026
- Status verified
- Oct 2026
- Primary completion
- Mar 31, 2028
- Completion
- May 31, 2028
Study Design
- Enrollment
- 192 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Usual Care
- Experimental: High Intensity Rehabilitation
- Experimental: Usual Care and STAMP
- Experimental: High Intensity Rehabilitation and STAMP
Primary Outcome Measure
Usual Gait Speed [ Time Frame: Admission into rehabilitation and discharge from rehabilitation, which would be an approximate average of 14 days ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Colorado Denver, Anschutz Medical Campus | Aurora | Colorado | 80045 | |
| Aegis Therapies | Frisco | Texas | 75034 |
Find similar trials in Aurora, CO
Related Studies
- Bioenergetic Effects of Aging and Menopause (BEAM)PHASE4 · Recruiting · University of Colorado, Denver · Aurora, Colorado
- Inspiratory Muscle Strength Training in Chronic Kidney DiseaseRecruiting · University of Colorado, Denver · Aurora, Colorado
- Inspiratory Muscle Strength Training for Lowering Blood Pressure and Improving Endothelial Function in Postmenopausal Women: Comparison With "Standard of Care" Aerobic ExerciseRecruiting · University of Colorado, Boulder · Boulder, Colorado
- Effects of Obesity in the AgedRecruiting · University of Texas Southwestern Medical Center · Dallas, Texas