ADJUNCTIVE EFFECT OF LIGHT EMITTING DIODE ON HAND GRIP STRENGTH IN BURN PATIENTS

Burns Clinical Trial

Official title:

ADJUNCTIVE EFFECT OF LIGHT EMITTING DIODE ON HAND GRIP STRENGTH IN BURN PATIENTS: A Randomized Controlled Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05212441
• Other study ID #: LEDHB2122
• Status: Active, not recruiting
• Phase: N/A
• Start date: February 25, 2022
• Est. completion date: July 10, 2022

Study information

• Verified date: May 2022
• Source: October 6 University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will be done to evaluate effect of applying LED before hand exercise on hand grip strength. Sixty male patients with subacute partial thickness burn of hand will be randomly allocated into two equal groups of 30 patients. The following equipment and tools will be used

Measurement equipments:

• For total active motion of fingers (TAM): Goniometer.

• For hand grip strength: Hand grip dynamometer.

Therapeutic equipment:

Light emitting diode therapy (LED) device.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 60
• Est. completion date: July 10, 2022
• Est. primary completion date: July 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 35 Years

Eligibility

Inclusion Criteria:

The subject selection will be according to the following criteria:

• Burn caused by thermal injury (flame or scald) with involvement of the wrist and hand and other parts of the body not including shoulder and elbow.

• Age range between 20-35 years.

• Male gender.

• Subacute Partial-thickness burn " From 3rd day of burn".

• Recent discharge of in patient acute care, spontaneous healing.

• All patients enrolled to the study will have their informed consent.

Exclusion Criteria:

The potential participants will be excluded if they meet one of the following criteria:

• Cardiac diseases.

• Perception of persistent respiratory problem related to a previous inhalation injury

• Signs of burn infection (i.e., unclear fluid oozing from the wound, increased pain, expanded redness and swelling)

• Exposed tendons.

• Nerve, muscle injury.

• Scar contracture of hand.

• Cognitive disorders.

• Presence of fractures.

• Patients who suffer from skin diseases, diabetes, varicose veins, and peripheral vascular diseases.

• Patients with life threatening disorders as renal failure, myocardial infarction or other similar diseases will be excluded from the study.

Related Conditions & MeSH terms

• Burns
• Hand Burn
• Hand Grasp
• Hand Injuries

Intervention

Device:
• Light emitting diode therapy (LED therapy)
The patient's forearm is positioned on table with palm facuing upward during the therapy. For LEDT, the center of the light spot located at approximately 50% of landmark line from the medial epicondyle to the styloid process of the ulna, which is the center belly of ?exor digitorum super?cialis. The subject's forearm maintained in the rest state without moving during the therapy. LED is performed before exercise.

Behavioral:
• Patient/family education program (Home program)
Patients and their families will instructed to learn the anti contracture positioning/splinting, scar massage and exercises program, application of the custom garments and inserts, and functional training to perform them on their own at home. Written and illustrative instructions and reciprocal demonstration sessions will be provided to the children and their families to ensure successful acquisition and delivery of rehabilitation skills at home program. The therapist will be reported about compliance with the home program every couple of days

Procedure:
• Positioning & Splinting
The wrist joint is splinted at 30 hyperextension, the MCP joint in 90 of flexion, the IP joints in extension, and the thumb in abduction. The webs of fingers kept in abduction. The hands are elevated above the level of the heart to minimize post-burn edema. Splinting: Splints are tailored to help to maintain the functional or anti-contracture position of the injured body parts.The intervals for monitoring vary from once every hour to once every 4-6 hours, depending on types of splints and skin conditions. It is described as 10 hours on and two hours off. When the splint is taken off, active and/or passive ROM should be carried out.

Other:
• Therapeutic Exercises
Passive ROM (PROM). Active ROM (AROM) & Active-assistive ROM (AAROM): The exercise will focus on extending the wrist to 45 degrees, flexing the MCP joints to 90 degrees and keeping the IP joints in full extension, while maintaining a thumb web space. The exercises will performed in the following sequences; (1) MCP joints flexion and extension with the wrist in neutral or slight extension and the IP joints in neutral position. (2) IP joints flexion to only 30-40 degrees with the wrist stabilized in the neutral or slight extension, while the MCP joints held in full extension, (3) thumb and fingers abduction and adduction, and (4) thumb opposition (tip of the thumb to tip of the small finger). Each exercise was performed for 8-10 repetition, daily, for 6 days/week. Stretching exercises: A low-load (low-intensity), long-duration stretch Strengthening exercises: done in static mode initially and progress to dynamic strengthening using elastic bands.

Locations

Country	Name	City	State
Egypt	October 6 University Hospital	Al ?ayy Ath Thamin	Giza

Sponsors (1)

Lead Sponsor	Collaborator
October 6 University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in Total active ROM from baseline to 6 weeks posttreatment	Total active ROM is the sum of the active metacarpophalangeal (MP), proximal interphalangeal (PIP), and distal interphalangeal (DIP) arc of motion in degrees of an individual digit. The measurement will be performed via a hand-held finger goniometer	baseline and 6 weeks posttreatment
Primary	Changes in hand grip strength from baseline to 6 weeks posttreatment	A calibrated hydraulic JAMAR (Model: 5030J1, Sammons Preston Rolyan, Chicago, USA), analogue hand-grip dynamometer will be used to measure grip strength. The device provides 1 kg increments on the measurement dial which faces the assessor as mentioned by Clifford et al., 2013.	baseline and 6 weeks posttreatment