App-Based rehab after joint replacement shows promise in early trial
NCT ID NCT07199478
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a WeChat mini-program that provides personalized rehab plans, progress tracking, and emotional support for people recovering from hip or knee replacement surgery. 140 adults aged 18-80 used the app alongside standard care, or standard care alone. The goal was to see if the app improves physical function and reduces pain at 6 weeks after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- WeChat-based mini-program for digital rehabilitation
- What this could lead to
- If it works, this could provide a simple, app-based way to improve recovery and quality of life after hip or knee replacement surgery.
- What could go wrong
- This is a small, single-center trial with 140 people. The app may not work for everyone, and results may not apply to other hospitals or patients without smartphones.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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140 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age: 18-80 years old. Surgery Type: Scheduled to undergo unilateral primary total hip arthroplasty (THA) or total knee arthroplasty (TKA). Physical Status: American Society of Anesthesiologists (ASA) classification I-III. Digital Literacy: Confirmed ability to use a smartphone via a standardized digital literacy test. Compliance: Willing and able to adhere to the study protocol. Exclusion Criteria: * Surgery Type: Revision surgery or simultaneous bilateral surgery. Cognitive Function: Presence of severe cognitive impairment (Mini-Mental State Examination (MMSE) score \<24). Arthritis Type: Inflammatory arthritis (e.g., rheumatoid arthritis). Psychological Status: Presence of depressive state at baseline (Hospital Anxiety and Depression Scale (HADS) depression subscale score ≥15).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Affiliated Hospital of Southwest Medical University
Luzhou, Sichuan, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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