sing a computerised test to monitor and compare recovery after hand surgery

Not Applicable

• Conditions: Injury, Occupational Diseases, Poisoning; Dupuytren's contracture, thumb-base osteoarthritis, carpal tunnel syndrome, trigger finger

• Registration Number: ISRCTN47966791
• Lead Sponsor: niversity of Oxford

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-07-18
• Last Update Posted: 12 August 2024
• Study Completion: 2026-12-16

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 396

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

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

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hand function measured using the Patient Evaluation Measure, administered via the EMCAT app daily for 12 weeks

Secondary Outcome Measures

Name	Time	Method
1. User engagement measured using the User Engagement Scale administered via the EMCAT app at 12 weeks<br>2. User engagement measured using response rates to EMCAT notifications administered via the EMCAT app over 12 weeks<br>