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Respiratory Muscle Strength, Endurance, and Postural Control in Chronic Neck Pain With Disability

Investigation of Respiratory Muscle Strength, Endurance, and Postural Control in Individuals With Non-Specific Chronic Neck Pain and Varying Degrees of Disability

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07124455
Acronym
ISU BT 1
Enrollment
60
Registered
2025-08-15
Start date
2024-04-04
Completion date
2024-11-01
Last updated
2025-08-15

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

Conditions

Neck Pain Chronic, Respiratory Function

Keywords

neck pain, respiratory function, neck disability, respiratory muscle strength, pain

Brief summary

Neck pain is a common cause of disability worldwide, especially among middle-aged women in wealthy countries. It often occurs in episodes and can become chronic, affecting physical, psychological, emotional, and social aspects of life, which reduces quality of life for both patients and their families. Research has shown that neck pain is linked to problems with movement control, such as reduced neck mobility, increased activity in surface muscles, and poor body position awareness. These issues may lead to breathing problems because surface neck muscles are involved in inhalation. Studies have found that people with chronic neck pain have reduced lung function and altered breathing patterns compared to healthy individuals. However, no research has yet explored how respiratory endurance and balance control relate to neck pain severity. This study will assess respiratory muscle strength, endurance, and postural control in people with chronic neck pain. Participants will be divided into groups based on the severity of their neck disability, and their respiratory and balance measurements will be compared to healthy individuals. The goal is to understand whether worsening neck disability is associated with greater respiratory problems.

Detailed description

This study designed as cross-sectional study. Aim The aim of this study is to investigate the presence of respiratory dysfunction in individuals with chronic non-specific neck pain by evaluating respiratory muscle strength, endurance, and postural control. It also aims to classify the data obtained according to the severity of neck disability and to determine whether respiratory dysfunction is associated with the severity of neck involvement. Research Hypotheses H0: There is no difference in respiratory muscle strength, endurance, and postural control parameters between individuals with chronic non-specific neck pain and asymptomatic individuals. H1: There is a difference in respiratory muscle strength, endurance, and postural control parameters between individuals with chronic non-specific neck pain and asymptomatic individuals. H2: The severity of chronic non-specific neck pain has no effect on the degree of respiratory impairment. H3: The severity of chronic non-specific neck pain has an effect on the degree of respiratory impairment. Specific Objectives of the Study To assess the severity of neck pain using the Neck Disability Index To measure the respiratory muscle strength of participants To measure the respiratory muscle endurance of participants To evaluate the postural control of participants To compare respiratory muscle strength, endurance, and postural control between individuals with neck pain and asymptomatic participants To examine the relationship between the severity of neck pain and the extent of respiratory dysfunction

Interventions

None listed

Sponsors

The Scientific and Technological Research Council of Turkey
CollaboratorOTHER
Istinye University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Individuals diagnosed with Non-Specific Neck Pain by a physician Having complaints of Non-Specific Neck Pain for at least 3 months Aged between 18 and 65 years Willingness to participate voluntarily No diagnosed respiratory disease No diagnosed cardiac disease No diagnosed neuromuscular disease Non-smoker

Exclusion criteria

Presence of radiculopathy or structural abnormalities in the cervical region History of surgery on the cervical region Upper respiratory tract infection within the last 3 months History of surgery involving the chest cage or spine Spinal deformities such as scoliosis or kyphosis History of abdominal surgery Inflammatory and rheumatological diseases Presence of infection in the bone or soft tissue of the cervical spine Presence of malignancy Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Maximum Expiratory Pressure4 weeksMaximum Expiratory Pressure is the intraoral pressure measured during maximum expiration against a closed airway valve. For the measurement, the participant first performs a maximum inspiration. Then, the airway valve is closed, and the participant performs maximum expiration, maintaining it for 1-3 seconds. The highest value out of three attempts will be selected and recorded in cmH₂O. Results will be expressed as a percentage of normal reference values calculated according to age and gender.
respiratory function test4 weeksLung function will be measured with a portable spirometer. The test will record forced vital capacity, the amount of air exhaled in one second, their ratio, and peak flow. Results will be given in liters and compared to predicted normal values. The test follows official guidelines and uses sterilized, personal mouthpieces to ensure safety.
Maximum Inspiratory Pressure4 weeksMaximum inspiratory mouth pressure is the intraoral pressure measured during maximum inspiration against a closed airway valve. For the measurement, the participant is asked to perform a maximum expiration first. Then, the airway valve is closed, and the participant performs a maximum inspiration, maintaining it for 1-3 seconds. The best value out of three attempts will be selected and recorded in cmH₂O. Results will be expressed as a percentage of normal reference values calculated according to age and gender.
Assessment of Cervical Disability:4 weeksCervical disability will be evaluated using the Turkish version of the Neck Disability Questionnaire. This is one of the most commonly used questionnaires for neck pain. It is used to assess the patient's current condition and progress during treatment. The questionnaire consists of 10 sections completed by the patient, covering pain, personal care, lifting heavy objects, reading, headaches, concentration, work, driving, sleeping, and recreation. Each section is scored from 0 (no disability) to 5 (complete disability). The total score ranges from 0 (no disability) to 50 (total disability). An increase in the score indicates greater disability, while a decrease indicates improvement. Based on the total score, disability is classified as follows: 0-4 points (0-8%) no disability, 5-14 points (10-28%) mild disability, 15-24 points (30-48%) moderate disability, 25-34 points (50-64%) severe disability, and 35-40 points (70-100%) complete disability (Vernon et al., 1991; Telci et al., 2009).
Measurement of Respiratory Muscle Endurance4 weeksRespiratory muscle endurance refers to the ability of the respiratory muscles to sustain performance during prolonged or repetitive contractions. This parameter is typically assessed with specific endurance tests and may vary depending on the measurement protocol. During the endurance test, the participant sustains respiratory muscle activity under a given load or intensity for a specified duration, and performance values are recorded.

Secondary

MeasureTime frameDescription
Anthropometric Measurements:4 weeksWaist circumference and chest circumference measurements at three different regions will be taken.
Postural Analysis:4 weeksFor postural analysis, the form developed by Corbin et al. will be used. Scoring will be performed according to the severity of postural deviations observed from the lateral and posterior views (Corbin et al., 2006).
Visual Analog Scale:4 weeksPerceived exertion, fatigue, and breathlessness will be assessed using the Visual Analog Scale (VAS) ranging from 0 (none) to 10 (very severe).
Assessment of Postural Control:4 weeksThe Functional Reach Test will assess postural control using a tape fixed to a wall. Participants stand close to the wall and reach forward with their dominant arm without stepping or lifting heels. Three trials will be done, averaging the last two. Before testing, handedness will be determined. Modified tests include reaching with both arms and on soft surfaces, as well as reaching sideways.
Borg Scale:4 weeksPerceived exertion, fatigue, and breathlessness will be assessed using modified Borg scale, ranging from 0 (none) to 10 (very severe).

Countries

Turkey (Türkiye)

Outcome results

None listed

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