Ignite Creation Date:
2024-05-06 @ 7:51 PM
Last Modification Date:
2024-10-26 @ 3:15 PM
Study NCT ID:
NCT06155617
Status:
COMPLETED
Last Update Posted:
2023-12-04
First Post:
2023-08-24
Brief Title:
Pain Range of Motion Edema Sensibility Strength PRESS Self-reported Function Create a Comprehensive Score
Sponsor:
Howard University
Organization:
Howard University
Study Overview
Official Title:
Development and Reliability of the PRESS to Function Approach A Systematic Method for Upper Extremity Assessment
Status:
COMPLETED
Status Verified Date:
2023-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PRESS
Brief Summary:
The aim of this study is to examine the development of a conceptual framework and provide evidence for reliability of a comprehensive hand therapy evaluation score This approach provides a new standardized tool for upper extremity UE evaluation Components of Pain Range of Motion ROM Edema Sensibility Strength PRESS and self-reported Function were combined to create a baseline Each assessment tool used for the PRESS to Function Approach assists in determining appropriate interventions
Detailed Description:
In this study investigators used the innovative PRESS to Function Approach and Composite Score to describe the development and piloting of a systematic standard for upper extremity evaluation Using existing instruments with substantial evidence of validity and reliability is more cost-effective than starting from scratch to develop and validate an instrument This Approach and Score will provide occupational therapists an accurate measure to track the progression of a patient The hypothesis for this study is Press to Function components will demonstrate utility for measuring clinical and patient-reported function when used as a comprehensive assessment tool
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None