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Thermotherapy in Acute Nonspecific Neck Pain

Comparison of the Short-term Effect of Superficial Thermotherapy Applications in Acute Nonspecific Neck Pain-Randomised Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06507761
Enrollment
60
Registered
2024-07-18
Start date
2024-07-10
Completion date
2025-07-10
Last updated
2024-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain, Cold

Brief summary

Neck pain is one of the most common musculoskeletal pain disorders secondary to low back pain. Medical and non-medical treatments such as physiotherapy are applied in its treatment. Patients with nonspecific neck pain (NBA) can be treated with various interventions such as drug therapy, manual therapy, heat and exercise. Although it is frequently used in clinical practice, there is no evidence that superficial thermotherapy (hot or cold) methods effectively relieve neck pain. Therefore, this study aims to compare the short-term effects of superficial hot or cold applications on pain, range of motion and functional status in patients with NBA.

Interventions

Cold pack application (2-4 degrees) will be wrapped in a towel and applied to the patient's back side neck and back for 15 minutes while the patient is lying prone.

OTHERSham

An unrefrigerated room temperature Cold Pack will be wrapped in a towel and applied to the patient's posterior neck and back for 15 minutes while the patient is lying face down.

OTHERHot Pack

Hot pack (55-60 degrees) application will be wrapped in a towel and applied to the back side neck and back of the patient for 15 minutes while the patient is lying face down.

Sponsors

Acibadem University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Being diagnosed with nonspecific neck pain by a doctor, * To be between the ages of 18-65, * Neck pain lasting for less than 1 month * No previous neck or shoulder surgery, * No shoulder pain due to any cause, * A tumour or inflammatory disease underlying the neck pain not to be found, * A clinically underlying stenosis or discogenic problem not to be present. * Negative results from the following clinical examination tests; Spurling test, Lhermitte test, Cervical distraction test, Adson test,

Exclusion criteria

* Not meeting the inclusion criteria, * Positive neurological examination (positive motor presence, reflex or sensory abnormalities indicating spinal root compression) or abnormal neurological findings related to nerve compression in the upper limb * Systemic rheumatological or metabolic diseases or cancer * Refusal to participate in the study, * Failure to complete treatment, * Having any neurological problem * Severe psychological illnesses

Design outcomes

Primary

MeasureTime frameDescription
The Numerical Rating Scale (NPRS-11)Change from baseline pain score at 3th dayThe Numerical Rating Scale (NPRS-11) is an 11-point scale for self-report of pain. It is the most commonly used unidimensional pain scale. The respondent selects a whole number (integers 0-10) that best reflects the intensity (or other quality if requested of his/her pain.0 point is the minimum and 10 point is the maximum. The higher the score, the more severe the pain.
Range of MotionChange from baseline range of motion at 3th dayCROM device will be used. The active range of motion of each individual will be measured and measured in accordance with the manufacturer's procedures
Global Rating of Change scale (Patient Satisfaction)Change from baseline Global Rating of Change scale at 3th dayPatient satisfaction regarding improvement in shoulder function will be evaluated by the Global Rating of Change scale. All participants will be asked to rate their condition after a six-week intervention period compared to baseline by indicating whether they have improved significantly, improved slightly, unchanged, deteriorated slightly, or deteriorated significantly between -3 to +3, with a higher value indicating better condition in this study.

Secondary

MeasureTime frameDescription
Neck disability indexChange from baseline disability scale at 3th daySince some parts of the 10-item questionnaire could not be answered by the patients (driving, working life), the average neck disability index score will be calculated by dividing the total score by the number of questions answered. The scoring is between 0 and 50. 0 points means the best result, 50 points means the worst result. 0 - 4 points; no disability, 5 - 14 points; mild disability, 15 - 24 points; moderate disability, 25 - 34 points; severe disability, \> 35 points; complete disability
Pressure Pain ThresholdChange from baseline Pressure Pain Threshold at 3th dayA digital pressure algometer will be applied to the web space of the foot opposite the trigger point. Participants are instructed to say stop or pain so the stimulus can be terminated when the sensation first transitions from pressure to pain (pain threshold).

Countries

Turkey (Türkiye)

Contacts

Primary ContactNuray ALACA
nuray.alaca@acibadem.edu.tr05324251290

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026