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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04291170
Other study ID # 55019
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 2021
Est. completion date December 2021

Study information

Verified date August 2021
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patient reported outcome measure (PROM) are a method by which to assess outcomes from a patient perspective. The QuickDASH is a commonly used PROM. QDASH was validated against grip strength and ability work, however not against its ability to actually measure what it sets forth to measure (ie: patient's ability to use a hammer, carry a shopping bag, wash a wall, etc). The purpose of this study is to correlate the self-reported QDASH with patients' ability to perform the functions on the QDASH and compare to a control group who completes the task on a lower extremity PROM, KOOS JR.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - new patient - stanford hand surgery clinic patient Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
QDASH
completing the tasks on the QDASH: open jar, wash wall, carry shopping bag, wash back, cut food, hammer wood
KOOSJR
completing tasks on the KOOSJR: pivot, straighten, go up/down stairs, stand upright, rise from sitting, bend over

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Outcome

Type Measure Description Time frame Safety issue
Primary QDASH score the quickdash is a validated outcome measure for hand function, scored 0-100 with higher scores indicating worse disability which is bad. Immediately after completing the taks
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