- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07565636
3D Printed Orthosis for Wrist Instability for Ehlers-Danlos Syndrome Patient
Custom Orthotic Using 3D Printed and 3D Scanned Method
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The purpose of this study is to examine the impact that a 3D-scanned and 3D-printed forearm wrist and hand orthosis has on function, pain and quality of life for people with Ehlers-Danlos Syndrome.
The goal of this research is to create a more supportive wrist hand orthosis for people with Ehlers-Danlos Syndrome (EDS) to prevent wrist dislocation using 3D scanning and 3D printing technologies with a biomedically safe material and address concerns for an underserved medical population. The investigators' goal is to create an orthosis that works better than the traditional ones by providing more support and decreasing pain for the participants with EDS. The investigators will create a custom 3D scanned and 3D printed wrist-hand orthotic for the participant and evaluate if there is a change on number of subluxation/dislocation due to Ehlers- Danlos syndrome as it relates to pain, activity participation and patient satisfaction. To assess this, the investigators will use patient-rated outcome measures, such as: the 0-100 Pain Scale, daily # of subluxation/dislocation occurrences, activity level via Health Assessment Questionnaire HAQ-D1, and the OPUS Satisfaction with Device and Services survey.
Aim 1: Develop a custom 3D-printed wrist-hand orthosis for participants with Ehlers-Danlos Syndrome (EDS) using 3D scanning and printing technologies.
The investigators will design and fabricate a custom orthosis tailored to each participant's unique anatomical needs using biomedically safe materials. The aim is to create an orthotic device that provides enhanced support to the wrist and hand, preventing subluxation and dislocation while minimizing pain compared to pre-fabricated orthoses.
Aim 2: Evaluate the effectiveness of the custom 3D-printed orthosis in changing the number of wrist subluxation/dislocation and changing the pain levels in participants with EDS.
The investigators will assess the effectiveness of the wrist-hand orthosis by measuring the frequency of subluxation/dislocation events and evaluating pain levels before and after wearing the device. The 0-100 Pain Scale will be used to quantify pain relief, and the occurrence of wrist subluxation/dislocation will be recorded to determine the device's impact on joint stability.
Aim 3: Assess the impact of the custom 3D-printed orthosis on activity participation and overall functional status in individuals with EDS.
The investigators will measure changes in activity levels and functional status using patient-reported outcome measures, including the Health Assessment Questionnaire HAQ-DI, and OPUS Satisfaction with Device and Services. These metrics will provide insight into the orthosis's ability to enhance participation in daily activities and improve overall quality of life for individuals with EDS.
Aim 4: Measure participant satisfaction with the custom 3D-printed orthosis. The investigators will use the OPUS Satisfaction with Device and Services survey to evaluate patient satisfaction with the orthosis. This will help determine whether the 3D-printed orthosis meets the unique needs and preferences of individuals with EDS in terms of comfort, functionality, and usability.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Erika Lewis, PT, EdD
- Telefonnummer: 978-934-4405
- E-mail: Erika_Lewis@uml.edu
Undersøgelse Kontakt Backup
- Navn: Yuko Oda, MFA, BA
- Telefonnummer: 978-934-3490
- E-mail: Yuko_Oda@uml.edu
Studiesteder
-
-
Massachusetts
-
Lowell, Massachusetts, Forenede Stater, 01854
- Rekruttering
- UMass Lowell, Expanded Media Fabrication Lab
-
Kontakt:
- Anna McCarthy, BFA
- Telefonnummer: 978-934-4294
- E-mail: Anna_McCarthy@uml.edu
-
Ledende efterforsker:
- Erika Lewis, PT, EdD
-
Ledende efterforsker:
- Yuko Oda, MFA, BA
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- English-speaking
- 21 or older
- Ehlers-Danlos syndrome
- wrist hypermobility
Exclusion Criteria:
- Under 21
- pregnant women
- prisoners
- non-English-speaking
- skin sensitivity
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Ehlers-Danlos Syndrome (EDS)
Individuals with EDS with symptoms of wrist subluxation or wrist dislocation causing limitation in participation in self-care and activities and social activities
|
Fabricate a Custom 3D scanned and 3D printed wrist-hand orthosis for a participant with EDS to measure the change in pain, number of daily wrist subluxation and change in participation in activities such as gardening and cooking.
The investigators will use participant feedback to customize the fit and design of the orthosis for maximum comfort and effectiveness.
The investigators are using HD (high definition) 3D scanning and 3D printing technology for a precise fit to prevent subluxation.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Wrist Joint Stability
Tidsramme: From enrollment to the end of intervention at 8 weeks
|
Change the frequency of daily wrist subluxations and dislocations over 8 weeks (0-100, lower number is better)
|
From enrollment to the end of intervention at 8 weeks
|
|
Change in Pain Rating in upper extremity for individuals with EDS
Tidsramme: From enrollment to the end of the intervention at 8 weeks
|
Change in pain as measured by the pain rating on the Health Assessment Questionnaire (HAQ-DI) (0-100 where 0=no pain and 100 = severe pain.
Lower number is better)
|
From enrollment to the end of the intervention at 8 weeks
|
|
Change in Activity Participation for individuals with EDS
Tidsramme: From enrollment to the end of intervention at 8 weeks
|
Change in participation in daily activities, as indicated by improvements in the Health Assessment Questionnaire (HAQ-DI) (The 8 scores of the 8 sections are summed and divided by 8.
The result is the DI or FDI, the disability index or functional disability index.
Each question can be rated 0-3 with 0 representing better functional ability.)
|
From enrollment to the end of intervention at 8 weeks
|
|
Satisfaction of person with EDS with 3D Scanned and 3D printed orthosis
Tidsramme: From Enrollment to the end of intervention at 8 weeks
|
Change in satisfaction levels as measured by the OPUS Satisfaction with Device and Services survey Satisfaction With Device Score is the sum of the scores for items 1-11 (11 - 55).
We will not use the "Satisfaction With Services Score is the sum of the scores for items 12-21 (10 - 50)".
The higher the score the better the outcome
|
From Enrollment to the end of intervention at 8 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Erika S Lewis, PT, EdD, University of Massachusetts, Lowell
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Muskuloskeletale sygdomme
- Karsygdomme
- Hjerte-kar-sygdomme
- Sår og skader
- Ledsygdomme
- Genetiske sygdomme, medfødte
- Bindevævssygdomme
- Hæmatologiske sygdomme
- Hudsygdomme
- Medfødte abnormiteter
- Hæmostatiske lidelser
- Hæmoragiske lidelser
- Hudsygdomme, genetisk
- Hudabnormiteter
- Kollagensygdomme
- Medfødte, arvelige og neonatale sygdomme og abnormiteter
- Hud- og bindevævssygdomme
- Hemiske og lymfatiske sygdomme
- Leddislokationer
- Ehlers-Danlos syndrom
- Ehlers-Danlos syndrom type 3
Andre undersøgelses-id-numre
- 23 (SIME)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
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