Evidence map›Paper›PMID 42553900›Full record

Trial reportClinics in orthopedic surgery2026

Digital Therapeutics for Postoperative Rehabilitation after Arthroscopic Rotator Cuff Repair: A Single-Center, Assessor-Blinded, Randomized Pilot Study.

So-Youn Chang, Jong-Ho Kim, Youn Kyu Lee, Hyun Tae Shin, Chul Ho Lee, Su Jeong Lee, Hong Kwon Lee, Min Jeon, Eun-Ji Yoon

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinics in orthopedic surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

So-Youn ChangDepartment of Rehabilitation Medicine, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-0040-8084
Jong-Ho KimOrthoCare, Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0000-0001-5475-1529
Youn Kyu LeeSchool of Computer Science and Engineering, Chung-Ang University, Seoul, Korea.ORCID https://orcid.org/0000-0002-4569-2640
Hyun Tae ShinOrthoCare, Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0009-0006-8432-5532
Chul Ho LeeOrthoCare, Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0009-0001-0812-7474
Su Jeong LeeOrthoCare, Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0009-0009-2333-4728
Hong Kwon LeeOrthoCare, Co., Ltd., Seoul, Korea.ORCID https://orcid.org/0009-0000-6443-9424
Min JeonSchool of Computer Science and Engineering, Chung-Ang University, Seoul, Korea.ORCID https://orcid.org/0009-0004-1170-545X
Eun-Ji YoonDepartment of Orthopedic Surgery, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-1614-4901

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Home-based rehabilitation after arthroscopic rotator cuff repair (ARCR) often lacks objective monitoring. To address this limitation, we developed the ANAPA digital rehabilitation (DR) system, which includes a patient-facing mobile application for clinical efficacy evaluation (ANAPA ME) and a physician-facing measurement application for technical assessment (ANAPA PS). This study compared the safety and preliminary efficacy of ANAPA ME with conventional YouTube-based rehabilitation (CR), with an additional validation of the automated measurement functions in ANAPA PS. Methods: This single-center, assessor-blinded, randomized pilot study included 18 patients who had undergone ARCR. The participants were allocated to the DR group (n = 9) or CR group (n = 9) and followed identical postoperative rotator cuff exercise protocols. The program was conducted for 24 weeks postoperatively. The shoulder range of motion (ROM), muscle strength, and clinical outcomes (visual analog scale pain score, Constant shoulder score, Shoulder Pain and Disability Index, and EuroQol-5 Dimension-5 Level questionnaire) were evaluated at baseline and at follow-up up to 24 weeks postoperatively. Ultrasonography was performed at 24 weeks to evaluate the integrity of the repaired tendons. Automated ROM and muscle strength measurements of ANAPA PS were validated against digital goniometry and hand-held dynamometry at the 6-month follow-up, and measurement consistency was assessed using intraclass correlation coefficients (ICCs) and coefficients of variation (CV). Results: Both the DR and CR groups demonstrated significant within-group improvements in ROM and clinical scores ( Conclusions: In this exploratory pilot study, the ANAPA DR system demonstrated favorable trends compared with CR in patients after ARCR, suggesting the feasibility and safety of artificial intelligence-based digital therapeutics in postoperative shoulder rehabilitation. The supplementary validation further demonstrated the technical reliability and measurement consistency of the ANAPA PS automated measurement functions for monitoring rehabilitation outcomes.

Indexed as

ArthroscopyExercise TherapyMobile ApplicationsRotator Cuff InjuriesAgedFemaleHumansMaleMiddle AgedMuscle StrengthPilot ProjectsRange of Motion, ArticularRotator CuffSingle-Blind MethodArthroscopyDigital therapeuticsMobile applicationRehabilitationRotator cuff tear

Identifiers

PMID42553900
PMCPMC13437144

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.