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 type | Interventional |
|---|---|
| Ages | 60 Years and up |
| Sex | All |
| Enrollment | 256 (estimated) |
| Sponsor | The University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | May 23, 2025 |
| Main results expected | March 1, 2028 |
| Study ends | March 1, 2030 |
| Registry record updated | April 6, 2026 |
| Trial ID | NCT06820021 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
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Postprandial drop and frailty in older adults having planned noncardiac surgery
This study tests whether a drop in blood pressure after meals and frailty predict low blood pressure after anesthesia starts in adults 65 and older undergoing planned noncardiac surgery.
-
Frailty Training for Emergency Nurses in Morocco
This trial tests whether a four-module training program helps Moroccan emergency nurses recognize and care for frail older adults in the ER.
-
Physical Function and Fall Risk in Older Adults in Lalín's Frailty Prevention Program
This study will look at how physical function and fall risk change in people 70 and older who participate in a routine frailty and falls prevention program, by comparing assessments before and after the 8–12 week program.
-
Home-based multicomponent exercise program for older adults with osteosarcopenia and frailty
This study tests a home-based exercise program built on the Fogg Behavior Model to see if it improves frailty, muscle strength, physical function, bone density, and quality of life in adults aged 60–85 with osteosarcopenia and frailty.
-
VIVI-OLIVE: Multicomponent Exercise and Olive Oil for Older Adults at High Risk of Falls
In adults 75 and older at high risk of falling, this study tests whether a 24-month plan of personalized exercise, Mediterranean diet guidance, and 60 mL of extra virgin olive oil daily can improve walking speed and reduce fall risk.
-
Frailty-focused prehabilitation before heart surgery
This study tests a home-based, frailty-tailored prehabilitation program for adults 65+ waiting 5 weeks or more for heart surgery to see if it improves fitness, frailty, heart-related function, nutrition, inflammation, quality of life, and hospital outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.