The Effect of Physiotherapy on Chronic Low Back Pain

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-26

Study Completion Date

2023-09-15

Brief Summary

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Demographic data of patients diagnosed with chronic low back pain and planned for medical treatment (n:30) and physical therapy in addition to medical treatment (n:30), as well as before and after treatment; Visual analog scale (VAS), Oswestry Disability Index (ODI) and Short form 36 (SF-36) quality of life scoring, Lumbar range of motion (LHA), straight leg raising test (DBK) and hand-finger ground distance (EPZM) were evaluated. Hot pack, transcutaneous electrical nerve stimulation (TENS) and ultrasound were given as physical therapy agents.

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Detailed Description

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Patients with VAS, ODI and SF-36 quality of life values before treatment, in addition to demographic data, who have applied to our Physical Medicine and Rehabilitation Policlinic in our hospital with chronic low back pain in the last 3 (three) months, are determined, and at least 30 above the age of 18 who received physiotherapy and who did not receive physiotherapy.

patient consents obtained and VAS, ODI and SF-36 quality of life values questioned.

Pre- and post-treatment values compared, and intragroup changes compared in both groups and evaluated whether physiotherapy contributes to pain, functionality and quality of life in treatment.

Conditions

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Chronic Low-back Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients with VAS, ODI and SF-36 quality of life values before treatment, in addition to demographic data, who have applied to our Physical Medicine and Rehabilitation Policlinic in our hospital with chronic low back pain in the last 3 (three) months, are determined, and at least 30 above the age of 18 who received physiotherapy and who did not receive physiotherapy. By calling the patient on the phone and being called to our hospital; patient consents will be obtained and VAS, ODI and SF-36 quality of life values will be questioned.

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Patients in both groups were evaluated after treatment by a physiatrist blinded to the study.

Study Groups

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Group 1

NSAID

Group Type ACTIVE_COMPARATOR

Nsaid

Intervention Type DRUG

Medical treatment

Group 2

nsaid and physiotherapy

Group Type ACTIVE_COMPARATOR

Nsaid

Intervention Type DRUG

Medical treatment

Phsiotheraphy

Intervention Type OTHER

Nsaid and phsiotheraphy (hotpack-ultrasound therapy- tens)

Interventions

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Nsaid

Medical treatment

Intervention Type DRUG

Phsiotheraphy

Nsaid and phsiotheraphy (hotpack-ultrasound therapy- tens)

Intervention Type OTHER

Other Intervention Names

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Medical treatment Medical treatment and phsiotheraphy

Eligibility Criteria

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Inclusion Criteria

* Patients who have been prescribed medical treatment or physiotherapy for mechanical back pain
* Those with demographic information as well as VAS, ODI information in their files
* Patients between the ages of 20-79 who applied to our hospital with the complaint of chronic low back pain

Exclusion Criteria

* Non-mechanical back pain
* Patients with physiotherapy contraindications
* Those with inflammatory diseases
* Severe heart failure
* Stroke, spinal cord injury, plegia due to traumatic brain injury
* A history of malignancy
* Active infection during treatment
* Having metal implants in the waist area
* Established osteoporosis
* Those with pacemakers

Minimum Eligible Age

20 Years

Maximum Eligible Age

79 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes