Recruiting

STAMP

Sponsor:

University of Colorado, Denver

Code:

NCT07872384

Conditions

Aging

Functional Recovery

Skilled Nursing Facility

Medically Complex

Deconditioning

Eligibility Criteria

Sex: All

Age: 50+

Healthy Volunteers: Not accepted

Interventions

High Intensity Rehabilitation

Safe Transfers and Mobility Program

Usual Care

Study Details

Brief summary:

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.

Conditions

Aging

Functional Recovery

Skilled Nursing Facility

Medically Complex

Deconditioning

Study ID

NCT07872384

Start date

Oct 1, 2026

Status verified date

Nov, 2026

Completion date

May, 2028

Anticipated

Primary completion date

Mar, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 50+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • At least 50 years old
  • Admitted to SNF from the hospital
  • Ambulatory at admission with minimal assistance or less

Exclusion Criteria:

  • Contraindications to high-intensity resistance training (per American College of Sports Medicine Exercise Testing and Prescription)
  • Neurological diagnosis (e.g., cerebral vascular accident, multiple sclerosis, Parkinson's disease, traumatic brain injury)
  • Lower extremity weight-bearing precautions that require greater than minimal assistance with ambulation
  • Subsequent SNF admission

Study Design

Enrollment

192 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Usual Care

experimental: High Intensity Rehabilitation

experimental: Usual Care and STAMP

experimental: High Intensity Rehabilitation and STAMP

Interventions

High Intensity Rehabilitation

An 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

The 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

Usual 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.

Primary outcome measure

  • Usual Gait Speed [ Time Frame: Admission into rehabilitation and discharge from rehabilitation, which would be an approximate average of 14 days ]

Central Contacts and Locations

Locations

Aegis Therapies

Recruiting

Frisco, Texas, United States, 75034

Contacts

More Information

Sponsor

University of Colorado, Denver

Last update posted

Nov 10, 2026

Last verified

Nov, 2026

Keywords

  • Rehabilitation
  • Older Adults
  • Physical Therapy
  • Occupational Therapy
  • i-STRONGER
  • High-Intensity Rehabilitation
  • Post-Acute Care
  • Physical Function
  • Safe Transfers and Mobility Program
  • Feasibility
  • Implementation Science

Trial information was received from ClinicalTrials.gov and was last updated on 2026-11-11. This information was provided to ClinicalTrials.gov by University of Colorado, Denver on 2026-11-10. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.