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Post-acute Multicomponent Frailty Intervention (FIT)

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Hebrew SeniorLife

Status

Completed

Conditions

Frailty

Treatments

Other: Multicomponent (Exercise + Protein Supplementation)

Study type

Interventional

Funder types

Other

Identifiers

NCT05906446
Pro00068129

Details and patient eligibility

About

The goal is to test feasibility of a frailty intervention, including exercises and nutritional supplementation.

Full description

The frailty intervention includes frequent short exercise sessions incorporating balance, resistance training, and walking to accommodate diminished endurance, with synergistic protein and nutritional supplementation, delivered on top of usual care in the post-acute Skilled Nursing Facility (SNF) setting. There is no control group.

Enrollment

50 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Community-dwelling before hospitalization
  • Age ≥ 65 years
  • Admitted to SNF directly from inpatient hospitalization
  • English speaking
  • Mild Frailty or worse, as measured by a Clinical Frailty Scale

Exclusion criteria

  • Discharged from Emergency Department
  • Non-community discharge plan on admission (e.g. plan to discharge to hospice)
  • Nothing per oral (NPO) dietary status
  • Presence of any feeding tube
  • Chronic kidney disease stage IV or worse
  • Clinician refusal
  • Inability or refusal to consume intervention products (e.g. allergies to protein supplement)
  • Inability to consent to study procedures

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Intervention
Experimental group
Description:
Regular exercise sessions incorporating balance, resistance training, and walking to accommodate diminished endurance, with synergistic protein and nutritional supplementation
Treatment:
Other: Multicomponent (Exercise + Protein Supplementation)

Trial contacts and locations

1

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Central trial contact

Sandra Shi, MD MPH

Data sourced from clinicaltrials.gov

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