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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06387927
Other study ID # PT-NEUR-10/2023-520
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2, 2023
Est. completion date February 20, 2024

Study information

Verified date April 2024
Source Ahram Canadian University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thirty male and female hypertension patients with chronic mechanical non-specific low back pain were included in this randomized controlled study conducted at the Ababa Private Physical Therapy Center in Beni-Seuf, Egypt. They were randomly assigned into two equal groups; the study group A control (n = 15) had a supervised conventional core stability, while the study group B (n = 15) received a home exercise program. In both groups' patients had evaluations before and after their six-week course of therapy. Modified-modified Schober test was used to assess the active back range of motion (ROM), Arabic version of Oswestry disability index (ODI) was utilized to evaluate functional disability, and visual analog scale (VAS) was used to measure pain.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 20, 2024
Est. primary completion date February 2, 2024
Accepts healthy volunteers No
Gender All
Age group 30 Years to 50 Years
Eligibility Inclusion Criteria: - hypertensive patient - patient with chronic back pain - The patients aged 30 to 50 years Exclusion Criteria: - Patients with vertebral fractures - patient with surgical spinal fixation - patient with rheumatic disorders - patient with systemic diseases - patient with multiple sclerosis.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
home exercise program
Patients in group B were taught the core stability exercise in the first visit they received Arabic printed booklet for exercise description repetitions with diagrams in addition to Arabic illustration videos, they received a weekly telephone call to ensure their compliance to the exercise & motivation.
the core stability exercise
supervised conventional core stability exercise

Locations

Country Name City State
Egypt Faculty of physical therapy Giza

Sponsors (1)

Lead Sponsor Collaborator
Ahram Canadian University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of pain Pain was assessed using the visual analog scale up to 4 weeks
Primary Assessment of lumbar flexion range of motion performed by modified modified schober test up to 4 weeks
Primary Assessment of functional disability performed by Oswestry disability questionnaire version 2.0 up to 4 weeks
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