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Lo studio clinico NCT07390227 per Sindrome della cuffia dei rotatori, Instabilità della spalla, Spalla congelata 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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Virtual Reality Intervention in Patients With Persistent Shoulder Pain 30 Domiciliare A domicilio Stile di vita Esercizio

Non ancora in arruolamento
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 NCT07390227 è uno studio interventistico per Sindrome della cuffia dei rotatori, Instabilità della spalla, Spalla congelata, attualmente non ancora in arruolamento. L'arruolamento dovrebbe iniziare il 12 gennaio 2026, con l'obiettivo di raggiungere 30 partecipanti. Sotto la guida di HAN University of Applied Sciences, dovrebbe concludersi entro il 1 dicembre 2026. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 9 febbraio 2026.
Sommario breve
Shoulder pain is very common and can make daily activities difficult. Many people have shoulder pain for a long time, even after treatment. Common shoulder problems include pain from the shoulder muscles and tendons, a frozen shoulder, or an unstable shoulder. Unfortunately, both surgery and physiotherapy often help only a little. This can be due to many reasons, such as people not continuing their exercises, fear of...Mostra di più
Descrizione dettagliata
For many people the long-term disability associated with musculoskeletal disorders (MSK) is substantial. Within this group of conditions, musculoskeletal shoulder problems are ubiquitous. They impact on sleep, social interaction, ability to perform activities of daily living, sporting participation, and work. The prevalence of MSK shoulder disorders is reported to range from 0.7% to 55.2%, with the incidence ranging ...Mostra di più
Titolo ufficiale

Virtual Reality Intervention in Patients With Persistent Shoulder Pain

Patologie
Sindrome della cuffia dei rotatoriInstabilità della spallaSpalla congelata
Pubblicazioni
Articoli scientifici e documenti di ricerca pubblicati su questo studio clinico:
Altri ID dello studio
  • ECO 721.11/25
Numero NCT
NCT07390227
Data di inizio (effettiva)
2026-01-12
Ultimo aggiornamento pubblicato
2026-02-09
Data di completamento (stimata)
2026-12-01
Arruolamento (previsto)
30
Tipo di studio
Interventistico
FASE
N.D.
Stato
Non ancora in arruolamento
Parole chiave
Virtual reality
Shoulder
persitent shoulder pain
Scopo principale
Trattamento
Allocazione
N.D.
Modello di intervento
A gruppo singolo
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
SperimentaleVR intervention arm
the intervention consists of educational video's, a simulation debriefing and VR exercises at home.
Exercise with Virtual reality
Participants exercise their shoulder at home with a VR headset, provided by the research team. The physiotherapist explains how to use the headset and wich applicatiosn should be used at which level. participants exercise daily 10 minutes for six weeks.
education on shoulder pain
participants receive a video-clip of 3 minutes that explains their shoulder condition.
simulation de-briefing
During the physiotherapy conultation, participants will be video-recorded with their own mobile device, when moving within VR. After thtat, the phyiotherapist and participant engage in a simulation de-briefing, discussing how it felt to move within VR, any changes in perceptions on pain and movement are discussed as well as the transfer to other movements in daily life.
Esito primario
Misure di esitoDescrizione della misuraArco temporale
The outcome measure belongs to the following areas of focus of feasibility 1) acceptability
acceptability: 1. recruitment rate defined as the number of participants who give their consent to the orthopaedic surgeon for an appointment with the research team to screen for eligibility 2. participation rate defined as the number of participants enrolled in the study divided by the number of eligible individuals approached 3. drop-out rate defined as the proportion of participants who discontinue the study before completing the 6-week VR program 3\. rate of response to questionnaires defined as the number of fully completed questionnaires at baseline and follow-up
From enrollment to the end of the treament 7 weeks
Assistente alla partecipazione
Criteri di eleggibilità

Età idonea
Bambino, Adulto, Adulto anziano
Età minima
16 Years
Sessi idonei
Tutti

  • General inclusion criteria:

    • Unilateral shoulder pain NPRS ≥ 4/10, persisting longer than 3 months

    • Adults ≥ 16 years old

    • Willing and able to comply with study protocol

    • Diagnosis of rotator cuff related shoulder pain, or shoulder instability, or frozen shoulder, confirmed according to international clinical guidelines

      1. RC related shoulder pain

    • shoulder pain and/or weakness during active or resisted shoulder external rotation, and or, shoulder elevation and/or

    • Presence of Painful arc during elevation

      2. shoulder instability

    • Radiographically, computed tomography scans, magnetic resonance imaging scans confirmed dislocation or

    • Documented history of manual or surgical relocation of the shoulder

    • Traumatic onset with persistent symptoms

    • Positive apprehension sign (fear of imminent dislocation when the arm is placed in abduction and external rotation during clinical examination)

      3. frozen shoulder

    • Restricted active and passive range of shoulder movement in all directions

    • Restricted active and passive shoulder external rotation of 50 percent compared to non-painful arm

    • Nothing abnormal detected on radiograph of shoulder

  • Neurological disease affecting the shoulder
  • Shoulder stiffness not consistent to frozen shoulder
  • Pain in the shoulder that is elicited by movements of the head and neck.
  • history of motion-sickness
  • history of seizures
  • severe vertigo or vestibular impairment.
HAN University of Applied Sciences logoHAN University of Applied Sciences
Netherlands Organisation for Scientific Research logoNetherlands Organisation for Scientific Research
Parte responsabile dello studio
Beate Dejaco, Investigatore principale, Principal Investigator at department Key Factors in Physical Activity and Rehabilitation Care, HAN University of Applied Sciences
Contatti principali dello studio
Contatto: Beate Dejaco, MSc, 0031622379871, [email protected]
Contatto: Niki Stolwijk, PhD, [email protected]
1 Centri dello studio in 1 paesi
HAN, Nijmegen, 6525 EN, Netherlands
Beate Dejaco, MSc, Contatto, 0622379871, [email protected]
Niki Stolwijk, PhD, Contatto, [email protected]