Wrist Splint and Occupational Therapy to Improve Pain, Mobility and Functional Status in Patients With Wrist Drop

Sponsor

Superior University (Other)

Overall Status

Recruiting

CT.gov ID

NCT05875844

Collaborator

(none)

Enrollment

Location

Arms

Anticipated Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

To determine effectiveness of wrist splint and occupational therapy to improve pain, mobility and functional status in patients with wrist drop.

Condition or Disease	Intervention/Treatment	Phase
Wrist-Drop	Diagnostic Test: Wrist Splint Diagnostic Test: Occupational Therapy	N/A

Study Design

Study Type:

Interventional

Anticipated Enrollment :

20 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Health Services Research

Official Title:

Effectiveness of Wrist Splint and Occupational Therapy to Improve Pain, Mobility and Functional Status in Patients With Wrist Drop

Actual Study Start Date :

Apr 1, 2023

Anticipated Primary Completion Date :

Jun 1, 2023

Anticipated Study Completion Date :

Aug 31, 2023

Arms and Interventions

Arm	Intervention/Treatment
Other: Wrist Splint	Diagnostic Test: Wrist Splint Wrist Splint to Improve Pain, Mobility and Functional Status in Patients With Wrist Drop
Experimental: Occupational Therapy	Diagnostic Test: Occupational Therapy Occupational Therapy to Improve Pain, Mobility and Functional Status in Patients With Wrist Drop

Arm

Intervention/Treatment

Other: Wrist Splint

Diagnostic Test: Wrist Splint

Wrist Splint to Improve Pain, Mobility and Functional Status in Patients With Wrist Drop

Experimental: Occupational Therapy

Diagnostic Test: Occupational Therapy

Occupational Therapy to Improve Pain, Mobility and Functional Status in Patients With Wrist Drop

Outcome Measures

Primary Outcome Measures

DASH scale (0-100) [6 Months]
DASH questionnaire for function on the scale of (0-100) worst zero- hundred normal
VAS on the scale (1-10) [6 Months]
VAS for pain for pain (0-10) 0 for normal, 10 for worst pain

Eligibility Criteria

Criteria

Ages Eligible for Study:

20 Years to 40 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

• People with wrist drop
People between 20 to 40 years will be included (male and female)
Post-operative patients (nerve grafting and plastic surgery)
Patients with findings of nerve compression will be included

Exclusion Criteria:

• People with nerve injuries other than radial nerve such as ulnar or median nerve
People suffering with other neurological disorders.
People who are not able to follow instructions
Any traumatic history
Diabetic patients, thyroid issues, pregnant females

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Chaudary Muhammad Akram Teaching Hospital	Lahore	Punjab	Pakistan

Sponsors and Collaborators

Superior University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Muhammad Naveed Babur, Principal Investigator, Superior University

ClinicalTrials.gov Identifier:

NCT05875844

Other Study ID Numbers:

DPT/Batch-Fall18/545

First Posted:

May 25, 2023

Last Update Posted:

May 25, 2023

Last Verified:

May 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Radial Neuropathy

Study Results

No Results Posted as of May 25, 2023