Comparison of Upper Extremity and Lower Extremity Function and Quick DASH

Sponsor
Stanford University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT04291170
Collaborator
(none)
0
2
3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: QDASH
  • Other: KOOSJR
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Comparison of Upper Extremity and Lower Extremity Function and Quick DAS
Anticipated Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: QDASH

Completing the tasks on the QuickDASH

Other: QDASH
completing the tasks on the QDASH: open jar, wash wall, carry shopping bag, wash back, cut food, hammer wood

Active Comparator: KOOSJR

Completing the tasks on the KOOSJR

Other: KOOSJR
completing tasks on the KOOSJR: pivot, straighten, go up/down stairs, stand upright, rise from sitting, bend over

Outcome Measures

Primary Outcome Measures

  1. QDASH score [Immediately after completing the taks]

    the quickdash is a validated outcome measure for hand function, scored 0-100 with higher scores indicating worse disability which is bad.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • new patient

  • stanford hand surgery clinic patient

Exclusion Criteria:

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Stanford University

Investigators

  • Principal Investigator: Robin N Kamal, MD MBA, Stanford University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Robin Kamal, Assistant Professor, Stanford University
ClinicalTrials.gov Identifier:
NCT04291170
Other Study ID Numbers:
  • 55019
First Posted:
Mar 2, 2020
Last Update Posted:
Aug 13, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 13, 2021