Dupuytren's contracture, thumb-base osteoarthritis, carpal tunnel syndrome, trigger finger Injury, Occupational Diseases, Poisoning
Conditions
Interventions
This is a mixed-methods cohort study to explore the feasibility of EMCAT for measuring between-group differences in postoperative recovery, its potential to guide follow-up type (face-to-face, telemed
Sponsors
University of Oxford
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Willing and able to give informed consent for participation in the study 2. Aged 18 years or older 3. Will undergo one of the eligible treatments 4. Willing and able to download and engage with the EMCAT application on their own personal device
Exclusion criteria
Exclusion criteria: 1. Undergoing bilateral treatments 2. Multiple treatments for the affected hand (for any condition) are planned within the study period 3. Unable to engage with the EMCAT application in the English language
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hand function measured using the Patient Evaluation Measure, administered via the EMCAT app daily for 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. User engagement measured using the User Engagement Scale administered via the EMCAT app at 12 weeks 2. User engagement measured using response rates to EMCAT notifications administered via the EMCAT app over 12 weeks | — |
Countries
England, Scotland, United Kingdom, Wales
Contacts
Public ContactConrad Harrison
Outcome results
None listed