Body Composition and Cervical Outcomes in Non-Specific Neck Pain

ConditionNeck Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorIzmir Democracy University

About this trial

Non-specific neck pain (NSNP) is a common musculoskeletal condition that significantly affects quality of life, daily activities, and work productivity. Although various physical, postural, and psychosocial factors have been associated with NSNP, the role of body composition in pain and functional outcomes remains unclear. Emerging evidence suggests that muscle and fat mass may influence musculoskeletal pain and related dysfunctions; however, studies examining these relationships in individuals with NSNP using objective measurements are limited. The purpose of this study is to investigate the effects of body composition on pain threshold, posture, cervical range of motion, sensation, and cervical function in individuals with non-specific neck pain. Individuals diagnosed with NSNP will be recruited from the Physical Medicine and Rehabilitation outpatient clinic. Participants' body composition, pain threshold, posture, cervical range of motion, sensory function, and cervical disability will be assessed using validated and objective measurement tools. Understanding the relationship between body composition and cervical outcomes in individuals with non-specific neck pain may contribute to early identification of risk factors and support the development of more targeted and effective physical therapy and rehabilitation strategies.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

To be between 18-65 years old

To be diagnosed with non-specific neck pain

Not having had any surgery related to the cervical region

Disqualifiers

Having a neurological and psychiatric problem that may affect evaluation methods

Pregnancy and pregnancy suspected

To be an elite athlete

Having a malignant disease

Trial design

Design model

Single group

Treatments tested in this trial

  • Clinical Assessment

    Other intervention

    Participants will undergo clinical assessments including body composition, pain threshold, posture, cervical range of motion, sensory function, and cervical disability. No therapeutic intervention will be applied.

Treatment groups

111 Participants
are divided into 1 treatment group
Group A: Non-Specific Neck Pain GroupOther 1 intervention

Trial outcomes

Primary outcomes

1

Total Body Weight

Total body weight (kg) will be measured using the Tanita BC-700 (Tanita, Japan) body composition analyzer, which uses single-frequency bioelectrical impedance analysis (BIA) technology.

Time frame
Baseline
2

Body Mass Index (BMI)

Body mass index (BMI, kg/m²) will be calculated automatically by the Tanita BC-700 based on measured body weight and participant-reported height entered into the device prior to measurement.

Time frame
Baseline
3

Total Body Fat Percentage

Total body fat percentage (%) will be assessed using the Tanita BC-700 body composition analyzer based on bioelectrical impedance analysis.

Time frame
Baseline
4

Lower Extremity Fat Percentage

Lower extremity fat percentage (%) will be measured using the Tanita BC-700 body composition analyzer.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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