NCT06898502

Investigation of Conservative Treatment Preferences of Patients With Chronic Low Back and Neck Pain

Completed NA Last updated 24 June 2025

What this trial tests

NA trial testing Electrotherapy ( TENS, hot pack, and therapeutic ultrasound ) in Chronic Low-back Pain (cLBP) in 100 participants. Completed in 29 May 2025.

Timeline

1 September 2024

Primary endpoint
29 May 2025

29 May 2025

Quick facts

Lead sponsor	Istanbul University - Cerrahpasa
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	na
Design	single group
Masking	none
Primary purpose	treatment
Enrollment	100
Start date	1 September 2024
Primary completion	29 May 2025
Estimated completion	29 May 2025
Sites	1 location across Turkey (Türkiye)

Drugs / interventions tested

• Electrotherapy ( TENS, hot pack, and therapeutic ultrasound )

Conditions studied

• Chronic Low-back Pain (cLBP) — all drugs for Chronic Low-back Pain (cLBP) →
• Chronic Neck Pain — all drugs for Chronic Neck Pain →

Sponsor

Istanbul University - Cerrahpasa

Who can join

18 and older, any sex, with Chronic Low-back Pain (cLBP) or Chronic Neck Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective: The aim of this study is to determine the preferences of individuals with chronic low back and neck pain regarding physiotherapy treatment methods and to examine the factors influencing these preferences. Additionally, the study aims to compare patient satisfaction, pain intensity, and disability levels between individuals who receive their preferred treatment and those who do not. Moreover, the relationships between patients' demographic characteristics, pain levels, pain beliefs, disability status, and depression severity with their preferred treatment methods will be investigated.

Materials and Methods: The study will include 50 patients with chronic low back and 50 patients with neck pain. In this study, four videos introducing commonly used physiotherapy and rehabilitation methods for the treatment of low back and neck pain (electrotherapy applications -TENS, ultrasound, hot pack-, manual therapy, kinesiotaping-dry needling, education, and exercise) will be prepared and shown to the participants. Pain intensity will be assessed using the "Numeric Pain Scale," pain beliefs with the "Pain Beliefs Scale," depression severity with the "Patient Health Questionnaire," and disability level with the "Oswestry Disability Index" for low back pain and the "Neck Disability Index" for neck pain. Participants will rank the treatment methods they watched and explain their reasons for preference. Each participant will receive electrotherapy treatment three times a week for four weeks. Each treatment session will consist of 20 minutes of TENS, 20 minutes of hot pack, and 6 minutes of ultrasound therapy. Twelve weeks after the treatment, participants will be contacted by phone and asked about their improvement using the "Global Rating of Change Scale (GRC)." Pain intensity and disability level will be reassessed through phone interviews using the "Numeric Pain Scale," the "Oswestry Disability Index" for low back pain, and the "Neck Disability Index" for neck pain at the 12th week. Thus, it will be evaluated whether there is any difference in patient satisfaction, pain intensity, and disability at the 12th week between participants who selected electrotherapy as the most effective method and those who chose other treatments. Statistical analysis of the data will be conducted using the SPSS program, and the analysis results will be presented with mean, standard deviation, frequency (%), number of patients (n), and confidence interval values. Treatment preferences and the factors influencing these preferences will be statistically examined, with a significance level of p\<0.05 considered statistically significant.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.