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Valutazione della Sicurezza e dell'Efficacia di un Dispositivo Terapeutico Digitale per Migliorare la Forza nella Sarcopenia (Sarc-DTx)

28 settembre 2026 aggiornato da: Exosystems

Uno Studio Clinico Multicentrico, Prospettico, Randomizzato, a Gruppi Paralleli, in Singolo Cieco, di Conferma per Valutare la Sicurezza e l'Efficacia di un Dispositivo Terapeutico Digitale per Migliorare la Forza Muscolare nei Pazienti con Sarcopenia

This clinical trial aims to demonstrate that the use of a digital therapeutic device (exoDTx) in patients with sarcopenia is superior to self-exercise in terms of muscle strength improvement and safety.

Panoramica dello studio

Stato

Attivo, non reclutante

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Background Sarcopenia is a condition characterized by progressive loss of skeletal muscle mass and strength, which is closely associated with functional decline, falls, and increased mortality.Conventional first-line treatment involves resistance training; however, in older adults, low adherence and practical challenges often limit its effectiveness.Recently, digital therapeutics (DTx) have emerged as promising tools by providing personalized exercise programs, automatic adjustment of intensity, and integrated recording and monitoring functions. These features are expected to overcome the limitations of selfdirected exercise.Therefore, this study seeks to validate the effectiveness and safety of DTx in improving muscle strength and physical function through a randomized controlled trial (RCT). Research Hypothesis In patients with sarcopenia, the group using digital therapeutics (DTx) will demonstrate superior outcomes in muscle strength improvement and safety compared to the self-exercise group.

Tipo di studio

Interventistico

Iscrizione (Stimato)

130

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Bucheon-si, Corea del Sud
        • Bucheon St. Mary's Hospital
      • Suwon, Corea del Sud
        • St.Vincent's hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 50 anni a 85 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria

  • Individuals diagnosed with sarcopenia according to both the European Working Group on Sarcopenia in Older People (EWGSOP) criteria and the Asian Working Group for Sarcopenia 2019 (AWGS 2019) criteria
  • Individuals with reduced muscle strength, defined as at least one of the following:
  • Handgrip strength < 28 kg for men or < 18 kg for women
  • Five-times Sit-to-Stand Test time > 12 seconds without arm support
  • Individuals with reduced muscle mass, defined as at least one of the following:
  • Skeletal Muscle Mass Index (SMI) < 7.0 kg/m² for men or < 5.4 kg/m² for women measured by DXA
  • Skeletal Muscle Mass Index (SMI) < 7.0 kg/m² for men or < 5.7 kg/m² for women measured by BIA
  • Individuals able to independently perform sit-to-stand movements
  • Individuals with sufficient physical and cognitive capacity to participate in the exercise program
  • Individuals able and willing to provide written informed consent
  • Individuals able to operate a mobile phone independently or with assistance from a caregiver

Exclusion Criteria

  • Individuals with cognitive impairment, defined as a Mini-Mental State Examination (MMSE) score < 20, or those unable to participate due to cognitive decline
  • Individuals with an implanted cardiac pacemaker or other implanted electronic medical device
  • Individuals with uncontrolled cardiovascular disease despite appropriate medical management
  • Individuals who have undergone lower-limb surgery within the past 6 months and are unable to ambulate independently
  • Individuals with moderate-to-severe musculoskeletal pain or functional limitations that interfere with objective functional assessments
  • Individuals with severe obesity, defined as a body mass index (BMI) > 50 kg/m²
  • Individuals currently receiving active cancer treatment or experiencing severe systemic frailty
  • Individuals with hemiplegia that prevents participation in the prescribed exercise program
  • Individuals who are anticipated by the investigator to be unable to complete the study procedures or follow-up assessments
  • Individuals unable to understand or comply with study instructions provided in Korean
  • Individuals considered unsuitable for study participation at the discretion of the investigator for any other reason

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Experimental Device Group (Home-based DTx exercise group after training)

Participants perform personalized resistance exercises using a digital therapeutic device (mobile application) at home for 12 weeks, with sessions conducted at least 3 times per week, 50 minutes per session (≥150 minutes/week). The program includes exercise automatic intensity adjustment, exercise recording/analysis, and physician monitoring

Experimental group (exoDTx): After baseline on-site training, participants perform personalized resistance exercises at home using a mobile app ≥3 times/week, 50 min/session, for 12 weeks (≥150 min/week). The program provides grip strength-based automatic intensity adjustment, exercise recording, feedback, and physician monitoring.

Delivery: Nonpharmacological, non-invasive, home-based exercise program. The experimental group uses a mobile app; the control group uses educational materials.

Initial instruction occurs on-site. Visits & Monitoring: Screening/Baseline (week 0), In-treatment (weeks 4, 8), Post-treatment (week 12), and Follow-up (week 24).

Comparatore attivo: Control Group (Self-exercise)

No mobile application is used. Participants perform the same type of exercise using QR code-based educational materials, self-regulating their exercise time, at least 3 times per week, 50 minutes per session, for a total of 12 weeks, with frequency and duration identical to the experimental group.

Control group (Self-exercise): No app is used. Participants perform the same exercise guided by QR code-based educational materials, ≥3 times/week, 50min/session, for 12 weeks, maintaining exercise logs without automatic adjustment or remote monitoring.

Delivery: Non-pharmacological, non-invasive, homebased exercise program. The experimental group uses a mobile app; the control group uses educational materials. Initial instruction occurs on-site. Visits & Monitoring: Screening/Baseline (week 0), In-treatment (weeks 4, 8), Post-treatment (week 12), and Follow-up (week 24).

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in peak knee extension strength (Nm) from baseline to 12 weeks
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

Between-group comparison of mean change in knee extensor strength measured by lower extremity dynamometer.

12 weeks after Visit 1 (treatment initiation)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in peak isometric knee extension strength (Nm) from baseline to 4, 8, and 24 weeks
Lasso di tempo: Baseline, 4 weeks, 8 weeks, and 24 weeks after Visit 1 (treatment initiation)

To evaluate longitudinal changes in knee extensor muscle strength at weeks 4, 8, and 24 compared with baseline using an lower extremity dynamometer.

Baseline, 4 weeks, 8 weeks, and 24 weeks after Visit 1 (treatment initiation)
Change in body composition (skeletal muscle mass index, fat mass)
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To evaluate changes in muscle and fat mass measured by dual-energy x-ray absorptiometry(DXA) or bioelectrical impedance analysis (BIA) after 12 weeks of intervention.

12 weeks after Visit 1 (treatment initiation)
Change in Manual Muscle Test (MMT) scores of major limb muscles
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To assess changes in muscle strength based on standardized MMT grading (0-5 scale) after 12 weeks of intervention..

12 weeks after Visit 1 (treatment initiation)
Change in handgrip strength (kg) from baseline
Lasso di tempo: Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks

To assess longitudinal changes in handgrip strength measured by hand dynamometer at weeks 4, 8, 12, and 24.

Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks
Change in calf circumference (cm) from baseline
Lasso di tempo: Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks

To assess longitudinal changes in calf circumference measured at the maximum girth of the dominant or less-affected lower leg at weeks 4, 8, 12, and 24.

Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks
Change in Muscle Function Index (MFI) from surface EMG analysis
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To quantify changes in muscle fatigue characteristics derived from surface electromyography (EMG) during resistance exercises.

12 weeks after Visit 1 (treatment initiation)
Change in Fugl-Meyer Assessment (upper/lower extremities; CNS-related sarcopenia subgroup)
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To examine motor recovery and coordination improvements using the Fugl-Meyer Assessment in participants with CNS-related sarcopenia.

12 weeks after Visit 1 (treatment initiation)
Change in 30-second chair stand test (repetitions) from baseline
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To assess changes in lower limb functional strength and endurance measured by the number of sit-to-stand repetitions completed in 30 seconds after 12 weeks of intervention.

12 weeks after Visit 1 (treatment initiation)
Change in Functional Ambulation Category (FAC) score
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To assess improvement in walking independence level using the Functional Ambulation Category (0-5 scale).

12 weeks after Visit 1 (treatment initiation)
Change in Berg Balance Scale (BBS) and Timed Up and Go (TUG) performance
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To evaluate dynamic and static balance performance using BBS score and TUG test time.

12 weeks after Visit 1 (treatment initiation)
Change in Short Physical Performance Battery (SPPB) total score and subscores (chair stand, gait speed, balance)
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To assess lower extremity function using SPPB, including 5-time chair stand, 6-meter gait speed, and balance tests.

SPPB - 5-time chair stand (time) 6-meter gait speed (SPPB gait speed) SPPB balance - score SPPB balance - time in seconds

12 weeks after Visit 1 (treatment initiation)
Change in Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls Questionnaire Score
Lasso di tempo: Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks

To assess changes in self-reported sarcopenia risk using the full Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls questionnaire. The SARC-F consists of 5 items, each scored from 0 to 2, resulting in a total score ranging from 0 to 10, with higher scores indicating worse sarcopenia severity and greater functional limitation.

Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks
Change in Sarcopenia Quality of Life score
Lasso di tempo: Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks

To measure sarcopenia-specific quality of life changes using Sarcopenia Quality of Life total score and domain subscores.

Sarcopenia Quality of Life contains 55 items generating a total score from 0 to 100, with higher scores indicating better quality of life.

Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks
Change in EuroQol Five-Dimension Five-Level (EQ-5D-5L) Questionnaire Score
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To assess changes in self-reported health-related quality of life using the full EuroQol Five-Dimension Five-Level (EQ-5D-5L) questionnaire. The EQ-5D-5L consists of 5 items, each scored from 1 to 5, resulting in a total score ranging from 5 to 25, with lower scores indicating better health-related quality of life and higher scores indicating greater health impairment.

12 weeks after Visit 1 (treatment initiation)
Change in Self-Efficacy for Home Exercise Programs Scale score
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To evaluate participants' confidence in independently performing prescribed home-based exercises.

12 weeks after Visit 1 (treatment initiation)
System Usability Scale (SUS) total score of the exoDTx mobile application
Lasso di tempo: 12 weeks after Visit 1 (treatment initiation)

To assess user satisfaction and perceived usability of the exoDTx digital therapeutic application using SUS.

12 weeks after Visit 1 (treatment initiation)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Investigatori

  • Investigatore principale: Sangui Choi, CPO, Exosystems

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

28 novembre 2025

Completamento primario (Effettivo)

23 settembre 2026

Completamento dello studio (Stimato)

10 dicembre 2026

Date di iscrizione allo studio

Primo inviato

20 novembre 2025

Primo inviato che soddisfa i criteri di controllo qualità

21 dicembre 2025

Primo Inserito (Effettivo)

6 gennaio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • HC25DDDS0072

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .