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Lo studio clinico NCT07486193 per Capsulite adesiva è non ancora in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui. | ||
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Università cinese di Hong KongEffects of Nunchaku Exercise for Improving Frozen Shoulder 50 Esercizio
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT07486193 è uno studio interventistico per Capsulite adesiva, attualmente non ancora in arruolamento. L'arruolamento dovrebbe iniziare il 30 marzo 2026, con l'obiettivo di raggiungere 50 partecipanti. Sotto la guida di l'Università cinese di Hong Kong, dovrebbe concludersi entro il 31 dicembre 2026. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 20 marzo 2026.
Sommario breve
The goal of this clinical trial is to investigate if nunchaku exercise works to treat adhesive capsulitis, or frozen shoulder in middle-aged or older adults. It will also learn about the adherence of this exercise intervention. The main questions it aims to answer are:
- Does practicing nunchaku exercises help reduce shoulder pain and improve shoulder movement?
- Do people stick with nunchaku exercises better, and s...
Descrizione dettagliata
Adhesive capsulitis, or frozen shoulder, is a progressive fibro-inflammatory condition characterized by synovitis, capsular thickening, and collagen remodeling, leading to substantial restrictions in active and passive shoulder motion. These movement limitations commonly result in impaired sleep, difficulties in self-care, and reduced capacity for work and leisure activities. Although conservative rehabilitation is t...Mostra di più
Titolo ufficiale
Effects of Nunchaku Exercise on Adhesive Capsulitis (Frozen Shoulder) in Middle-aged and Older Adults: A Randomized Controlled Trial
Patologie
Capsulite adesivaAltri ID dello studio
- FS_nun_1
Numero NCT
Data di inizio (effettiva)
2026-03-30
Ultimo aggiornamento pubblicato
2026-03-20
Data di completamento (stimata)
2026-12-31
Arruolamento (previsto)
50
Tipo di studio
Interventistico
FASE
N.D.
Stato
Non ancora in arruolamento
Parole chiave
Frozen Shoulder
Nunchaku exercise
adhesive capsulitis
Nunchaku exercise
adhesive capsulitis
Scopo principale
Trattamento
Allocazione
Randomizzato
Modello di intervento
In parallelo
Mascheramento
Singolo
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
Comparatore attivoShoulder Mobilization and Stretching Exercise (SMSE) | Shoulder Mobilization and Stretching Exercise (SMSE) Participants in this group will be offered a 12-week rehabilitation program consisting of two 60-minute sessions per week. This program has been designed by a registered physiotherapist in accordance with the Hospital Authority of Hong Kong's self-care guidelines. Each session includes joint mobilization exercises, end-range stretching using a towel or stick, and muscle-strengthening and stabilizing exercises. The tr...Mostra di più |
SperimentaleNunchaku Exercise | Nunchaku exercise Participants randomized to the Nunchaku Exercise group will participate in a 12-week training program consisting of two 60-minute sessions per week. To prioritize safety and minimize the risk of injury, you will use a soft towel with a knot at each end to simulate nunchaku movements (Figure 1). The training focuses on the level one syllabus of the standard nunchaku system, which involves rhythmic multi-angle movement...Mostra di più |
Esito primario
Esito secondario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Shoulder Pain and Disability Index (SPADI) | SPADI will be used to assess shoulder pain and functional limitations during daily living activities. SPADI, comprising 5 items to assess pain and 8 to assess disability, is widely used to evaluate the negative impact of frozen shoulder. Its Chinese version has been validated in China with good internal consistency and reliability | From enrollment to the end of follow-up period at 24 weeks |
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Visual Analog Scale for Pain (VAS) | The perception of pain during resting, and ordinary daily activities will be assessed using VAS. Participants will be instructed to draw a mark on a 10-cm line, with one end indicating no pain and the other indicating worst pain imaginable, to indicate their pain level | From enrollment to the end of follow-up period at 24 weeks |
Constant-Murley Score (CMS) | Overall shoulder function will be assessed using the CMS. CMS assesses 4 domains, including pain, how shoulder function affects daily activity, pain-free range of motion, and muscle strength. This instrument has been validated in China. This assessment will be conducted by a registered physiotherapist. | From enrollment to the end of follow-up period at 24 weeks |
Pain-free Range of Motion (ROM) | The pain-free ROM of forward and lateral elevation during flexion and abduction will be measured using a goniometer. The assessment will be conducted by a registered physiotherapist. | From enrollment to the end of follow-up period at 24 weeks |
Enjoyment of intervention | Enjoyment of intervention will be assessed using the Eight-Item Physical Activity Enjoyment Scale (PACES-8). | From mid-intervention at 6 weeks to to the end of follow-up period at 24 weeks |
Assistente alla partecipazione
Criteri di eleggibilità
Età idonea
Adulto, Adulto anziano
Età minima
45 Years
Sessi idonei
Tutti
- Ethnic Chinese;
- Age 45 years or above;
- Diagnosed with Adhesive Capsulitis (Frozen Shoulder) and currently in the thawing stage.
- Presence of secondary causes of shoulder stiffness, including recent trauma, post-surgical stiffness, or structural lesions such as full-thickness rotator cuff tears or severe glenohumeral arthritis;
- Receipt of recent shoulder treatments known to influence short-term outcomes, including corticosteroid injections within the past three months, hydrodilatation, manipulation under anesthesia, arthroscopic capsular release within the past six months, or structured shoulder physiotherapy within the past three months;
- Presence of somatic conditions that limit their ability to participate safely in exercise (e.g., inability to walk without an assistive device).
Università cinese di Hong Kong474 studi clinici attivi da esplorareParte responsabile dello studio
Angus Pak-Hung Yu, Investigatore principale, Research Assistant Professor, Chinese University of Hong Kong
Contatti principali dello studio
Contatto: Angus Pak-Hung Yu, PhD, (852) 39435253, [email protected]
1 Centri dello studio in 1 paesi
Department of Sports Science and Physical Education, The Chinese University of Hong Kong, Hong Kong, Hong Kong
Angus Pak-Hung Yu, PhD, Contatto, (852) 39435253, [email protected]