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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05904990
Other study ID # p.t.REC\012\004507
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 29, 2023
Est. completion date September 1, 2023

Study information

Verified date March 2024
Source October 6 University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will be conducted to investigate High-intensity laser therapy improves pain, health status and quality of life in women with fibromyalgia


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date September 1, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 55 Years
Eligibility Inclusion Criteria: 1. WPI = 7/19 pain sites and SSS = 5/12 or WPI between > 3-6/19 and SSS > 9/12 2. symptoms have been present at a similar level for at least 3 months 3. the patient does not have another disorder that would otherwise sufficiently explain the pain 4. generalized pain, defined as pain in at least four of five regions, is present Exclusion Criteria: - uncontrolled diabetes - known history of cancer

Study Design


Related Conditions & MeSH terms


Intervention

Device:
traditional exercise therapy only
50-minute program included a 10-minute warm-up phase (treadmill walking at a comfortable speed), 30 minutes of stretching exercises for (glutei, paraspinal muscles, hamstring, pectoralis, scalenus, intercostal muscles, and trapezius), and a 10-minute cool-down involving self-stretching and respiratory exercises
HILT alongside traditional exercise therapy
YAG laser device (HIRO 3.0; ASA Laser, Arcugnano, Italy). This equipment delivers pulsed laser light at a wavelength of 1,064 nm, with a very high peak power of 3 kW and energy density ranging from 360 to 1,780 mJ/cm2. It operates with short pulse durations between 120 and 150 µs, at low frequencies of 10 to 40 Hz, and has a duty cycle of about 0.1%.

Locations

Country Name City State
Egypt Kerolous Ishak Shehata Kelini 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 Revised Fibromyalgia Impact Questionnaire (FIQR) assesses the overall severity of FM and health status based on participant ratings. It encompasses three key domains similar to the FIQ (function, overall impact, and symptoms), with additional inquiries regarding memory, tenderness, balance, and environmental sensitivity up to 6 weeks
Primary Visual Analog Scale (VAS) 10 cm, where patients rated their pain on a scale from 0 ("no pain") to 10 ("extremely severe pain ") over the past 3 days up to 6 weeks
Primary pressure algometer This tool comprises a circular rubber tip (1 cm2) and a pressure gauge for displaying readings in kilograms. Given the rubber tip's 1 cm² area, measurements were reported in kilograms per square centimeter (kg/cm2). The algometer has a measurement range from 0 to 10 kg, with increments of 0.1 kg. The instrument was pressed against the skin's surface at a right angle, and the force exerted was registered on a manometer. up to 6 weeks
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