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Virtual Reality Intervention in Patients With Persistent Shoulder Pain 30 Häuslich Zu Hause Lebensstil Bewegung

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Die klinische Studie NCT07390227 ist eine interventionsstudie zur Untersuchung von Rotatorenmanschetten-Syndrom, Schulterinstabilität, Schultersteife und hat den Status noch nicht rekrutierend. Der Start ist für 12. Januar 2026 geplant, bis 30 Teilnehmer aufgenommen werden. Durchgeführt von HAN University of Applied Sciences wird der Abschluss für 1. Dezember 2026 erwartet. Die Daten von ClinicalTrials.gov wurden zuletzt am 9. Februar 2026 aktualisiert.
Kurzbeschreibung
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...Mehr anzeigen
Ausführliche Beschreibung
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 ...Mehr anzeigen
Offizieller Titel

Virtual Reality Intervention in Patients With Persistent Shoulder Pain

Erkrankungen
Rotatorenmanschetten-SyndromSchulterinstabilitätSchultersteife
Publikationen
Wissenschaftliche Artikel und Forschungspapiere zu dieser klinischen Studie:
Weitere Studien-IDs
  • ECO 721.11/25
NCT-Nummer
NCT07390227
Studienbeginn (tatsächlich)
2026-01-12
Zuletzt aktualisiert
2026-02-09
Studienende (vorauss.)
2026-12-01
Geplante Rekrutierung
30
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Noch nicht rekrutierend
Stichwörter
Virtual reality
Shoulder
persitent shoulder pain
Primäres Ziel
Behandlung
Zuteilungsmethode
Nicht zutreffend
Interventionsmodell
Einarmige Studie
Verblindung
Keine (offene Studie)
Studienarme/Interventionen
Teilnehmergruppe/StudienarmIntervention/Behandlung
ExperimentellVR 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.
Hauptergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
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
Teilnahme-Assistent
Eignungskriterien

Zugelassene Altersgruppen
Kind, Erwachsene, Ältere Erwachsene
Mindestalter
16 Years
Zugelassene Geschlechter
Alle

  • 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
Verantwortliche Partei
Beate Dejaco, Hauptprüfer, Principal Investigator at department Key Factors in Physical Activity and Rehabilitation Care, HAN University of Applied Sciences
Zentrale Studienkontakte
Kontakt: Beate Dejaco, MSc, 0031622379871, [email protected]
Kontakt: Niki Stolwijk, PhD, [email protected]
1 Studienstandorte in 1 Ländern
HAN, Nijmegen, 6525 EN, Netherlands
Beate Dejaco, MSc, Kontakt, 0622379871, [email protected]
Niki Stolwijk, PhD, Kontakt, [email protected]