Investigation of the Effectiveness of Tecar Therapy in Patients With Chronic Neck Pain

Not Applicable

Not yet recruiting

• Conditions: Neck Pain

• Registration Number: NCT06953973
• Lead Sponsor: Kirsehir Ahi Evran Universitesi

Brief Summary

Study Design This study was planned as a randomized controlled, double-blind study. Chronic neck pain diagnosed by a specialist physician will be divided into 3 groups with a randomization model. Interested individuals will be included in the study if they meet the inclusion criteria and sign the 'Informed Voluntary Consent Form' after the study is explained.

Patients will be divided into 3 groups with a randomization (secretary not in the study) model.

Patients who choose 1 will be applied Tecar Therapy + Standard Physiotherapy Program (SFP), those who choose 2 will be applied Sham Tecar Therapy +SFP and those who choose 3 will be applied SFP. The first and last evaluations of all 3 groups will be made by the same blind evaluator.

Randomization After the study is explained to the patients with chronic neck pain who meet the inclusion and exclusion criteria, those who volunteer will be asked to sign the "Informed Voluntary Consent Form". Those who volunteer to participate in the study will be randomly assigned to Group 1, Group 2 or 3. Participants will be randomly assigned to a card. Those who draw number 1 will be assigned to the SFP+Tecar Therapy group, those who draw number 2 will be assigned to the Sham Tecar Therapy + SFP group, and those who draw number 3 will be assigned to the SFP only group.

Visual Analog Scale (VAS) The pain intensity felt by the participants in the knee joint during rest and activity will be evaluated with VAS. VAS is an easy-to-use scale as it does not have any language and is frequently applied in clinics. Individuals will be asked to describe the pain they feel during the test on a 10 cm scale as "0" (no pain) and "10" (unbearable pain). A 34% decrease in VAS after TKA is considered clinically significant.

Neck Disability Index Neck Disability Index (NDI) was developed by Vernon et al. The Turkish version study was conducted by Aslan et al. The NDI includes a total of 10 questions such as pain, personal care, concentration, work, driving, and sleeping. Each question is scored between 0 and 5 points. A score of 0 means no restriction, and a score of 50 means full restriction. A score between 0-4 indicates no restriction, a score between 5-14 indicates mild restriction, a score between 14-24 indicates moderate restriction, a score between 25-34 indicates severe restriction, and a score above 35 indicates restriction.

Tampa Kinesiophobia Scale TKÖ is a 17-question checklist and is used in acute and chronic low back pain, fibromyalgia, musculoskeletal injuries, and whiplash-related diseases. The scale uses a 4-point Likert scale (1= I strongly disagree, 4= I strongly agree). A total score is calculated after reversing items 4, 8, 12, and 16. The person receives a total score between 17-68. A high score on the scale indicates that the person has high kinesiophobia. The validity and reliability of the questionnaire in Turkish was conducted by Tunca Yılmaz et al.

Quality of Life (SF-12) SF-12 consists of 8 sub-dimensions and 12 items, including physical functioning (2 items), physical role (2 items), body pain (1 item), general health (1 item), energy (1 item), social functioning (1 item), emotional role (2 items) and mental health (2 items). While the items related to physical and emotional role are answered dichotomously (yes or no), other items have Likert-type options ranging from 3 to 6. The total score of the survey varies between 0-100, with higher scores representing better health. The validity and reliability of the survey in Turkish was performed by Soylu et al.

Hospital Anxiety Depression Scale The scale is used to determine the risk of anxiety and depression in patients, and to measure their levels and changes in severity. The scale consists of a total of 14 questions. Seven of these (odd numbers) measure anxiety, while the other seven (even numbers) measure depression. The scale provides a four-point Likert-type measurement. Each item is scored differently. Items 1, 3, 5, 6, 8, 10, 11 and 13 show decreasing severity and are scored in the form of 3, 2, 1, 0. On the other hand, items 2, 4, 7, 9, 12 and 14 are scored in the form of 0, 1, 2, 3. The total scores of the subscales are obtained by adding these item scores. While items 1, 3, 5, 7, 9, 11 and 13 are added for the anxiety subscale, the scores of items 2, 4, 6, 8, 10, 12 and 14 are added for the depression subscale. Each heading is scored between 0-21. High scores indicate high anxiety and depression. The Hospital Anxiety and Depression Scale was developed by Zigmond and Snaith in 1983. In our country, the validity and reliability study was conducted by Aydemir in 1997.

Global Rating Of Change Scale This scale is frequently used to evaluate patient satisfaction in orthopedic clinical studies. It is designed to determine the amount of improvement or deterioration of the patient over time. In GRC, which is a Likert-type scale, the options in the plus and minus value ranges and the labels assigned to these degrees

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-04
• Study First Submitted: 2025-04-24
• Study First Submitted QC: 2025-04-24
• Study First Posted: 2025-05-01
• Last Update Submitted: 2025-05-20
• Last Update Posted: 2025-05-21
• Study Start: 2025-06-02
• Primary Completion: 2025-11-01
• Study Completion: 2026-02-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 69

Inclusion Criteria

• Being between the ages of 18-55,
• Having neck pain for 3 months or longer,
• Being able to come to the hospital for a standart physiotherapy program

Exclusion Criteria

• Patients who have had a cervical spine injury or surgery
• Patients with neck pain secondary to a neurological or vascular disorder or neoplasia
• Patients with radiculopathy and neurological deficits
• Patients with a history of inflammatory or infective arthritis in the cervical spine
• Patients who have received a physical therapy program in the last 6 months
• Patients with open wounds or risk of infection.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Visual Analog Scale (VAS)	0-4 weeks
Neck Disability İndex	0-4 weeks

Secondary Outcome Measures

Name	Time	Method
Tampa Kinesiophobia Scale	0-4 weeks
Short Form-12 (SF-12)	0-4 weeks
Hospital Anxiety Depression Scale	0-4 weeks
Global Rating Of Change Scale-GRC	0-4 weeks

Trial Locations

Locations (1)

Kırşehir Ahi Evran University; 🇹🇷 Kırşehir, Center, Turkey