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Pain, Range of Motion, Edema, Sensibility, Strength (PRESS) & Self-reported Function Create a Comprehensive Score

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Howard University

Status

Completed

Conditions

Upper Extremity Problem
Hand Injuries and Disorders

Treatments

Other: Upper Extremity Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT06155617
IRB-20-PNAH-08

Details and patient eligibility

About

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.

Full 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.

Enrollment

30 patients

Sex

All

Ages

21 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of upper extremity disorder as the primary diagnosis
  • Surgical and nonsurgical Diagnoses
  • Age 21 years or older

Exclusion criteria

  • Concomitant Diseases (i.e cerebralvascular accident, cerebral palsy, spinal cord injury)
  • Full Body Lymphedema
  • Individuals who did not complete at least one reassessment

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Single Arm Clinical Trial
Other group
Description:
Participants with various upper extremity disorders are provided treatment/interventions and evaluated at baseline, 3-6 weeks, and at discharge using the PRESS to Function Approach
Treatment:
Other: Upper Extremity Rehabilitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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