Clinical trial Recruiting at 1 site Interventional Ages 60 and up

Home-based strength program for older adults recovering from a hospital stay

Official title: The Effects of a Strength-based Tailored-Exercise Program at Home (STEP@Home) on Health Outcomes of Geriatric Patients at Risk of Hospitalization-associated Functional Decline: A Sequential Mixed-method Study

Run by The University of Hong Kong · NCT06820021 · Data updated 2026-11-12

This tests a 20-week, strength-focused, personalized home exercise program for older adults at risk of losing function after a hospital stay.

Quick facts

Study typeInterventional
Ages60 Years and up
SexAll
Enrollment256 (estimated)
SponsorThe University of Hong Kong
Academic / other
Locations1 site (Hong Kong)
StatusRecruiting
StartedMay 23, 2025
Main results expectedMarch 1, 2028
Study endsMarch 1, 2030
Registry record updatedApril 6, 2026
Trial IDNCT06820021 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 60 or older who had an acute hospital stay of at least two days, are discharged home without exercise-based rehab referral, score above the SHERPA threshold indicating risk of post-hospital functional decline, own a smartphone, and consent to participate.

Probably not a fit

Patients who are bed-bound, have disabling conditions causing major functional loss (e.g., recent stroke), have acute unstable cardio-respiratory or musculoskeletal contraindications to exercise, or already do moderate-to-vigorous exercise over 60 minutes per week are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a sequential mixed-method trial that randomizes eligible older adults 1:1 to a 20-week Strength-based Tailored-Exercise Program at Home (STEP@Home) or to standard physical activity education, using block randomization. The quantitative phase is a randomized controlled comparison of physical function and health-related quality of life outcomes, followed by a qualitative phase of interviews to explore participants' experiences and engagement. The intervention uses empowerment strategies, lifestyle-integrated functional exercises, and tele-platform video calls via smartphone to support sustainable self-practice after discharge. The design targets hospitalization-associated functional decline by delivering tailored strength training at home and measuring real-world feasibility and effects.

Why it matters

Potential benefit: If successful, the program could help older adults regain or maintain physical function and quality of life after hospitalization and may reduce downstream healthcare use.

How similar studies have gone: Previous home-based and telerehabilitation programs for older adults have shown improvements in mobility and function, though strength-based, tailored post-discharge programs with a mixed-methods evaluation are less common.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* i) aged 60 or above
* ii) has an acute hospitalization and the length of hospital stay is of ≥ 2 days2,
* iii) has risk of functional decline in 3 months following hospitalization as measured by the Screening for High-Risk Patients (SHERPA) score of \>3.5. SHERPA is a brief measure to identify the high risk by screening for the risk factors, including old age, poor health perception, IADL dysfunction, mild cognitive impairment and fall in the previous year.
* iv) discharged home without any referral for exercise-based rehabilitation
* v) has a Smartphone to access video calls
* vi) consented to participate.

Exclusion Criteria:

* i) admitted with a disabling condition leading to significant functional loss such as stroke,)
* ii) bed-bound or chair bound
* iii) with conditions contradictory to exercise training (e.g., acute muscular-skeletal problem, acute and unstable cardio-respiratory disease, etc),
* iv) engaging in moderate or vigorous exercise (\>60min/week) in the past 6 months.

Where it's running

  • the University of Hong Kong
    Hong Kong, Hong Kong
    Recruiting

Study contacts

  • Principal investigator: Doris Sau Fung YU, PhD — The University of Hong Kong
  • Study coordinator: Doris Sau Fung YU, PhD
  • Email: dyu1@hku.hk
  • Phone: 39176319

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.