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NCT03779958 Clinical Trial

Alternatives to Hand Therapy for Hand Surgery Patients

Carpal Tunnel Syndrome Clinical Trial

Official title:
Alternatives to Hand Therapy for Hand Surgery Patients

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT03779958
Other study ID # 47777
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 12, 2019
Est. completion date June 2023

Study information
Verified date July 2021
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients will be asked to use a mobile phone app to conduct their hand therapy after having hand surgery.

Description:

Patients who are undergoing the included procedures will be informed of the study & consented. They will be given information on how to download the app & input their surgery date. The app will guide the patient through various hand therapy exercises and ask them to record their QuickDASH, PSFS and VAS Pain weekly.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date June 2023
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - patients undergoing the following procedures: carpal tunnel release, trigger finger release, distal radius fracture fixation, de quervains release, cyst excision, finger fracture fixation - smart phone that is compatible with the app Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Mobile App
a mobile app that demonstrates hand therapy exercises

Locations
Country Name City State
United States Stanford Health Care Redwood City California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary QuickDASH The QD is a short form of the DASH, which measures disability of the arm, shoulder and hand. it is scored 0-100, with higher scores indicating higher disability once a week for 6 weeks
Secondary Patient Specific Functional Scale the PSFS is a validated measure of disability, that is scored on a 0-10 scale with lower scored indicating higher disability. once a week for 6 weeks
Secondary VAS Pain VAS pain is a validated measure of pain, scored 0-10, with higher scores indicating higher pain once a week for 6 weeks
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