- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07684092
Diaphragmatic Breathing and Electroacupuncture for Chronic Neck Pain
Diaphragmatic Breathing and Electroacupuncture in Patients With Chronic Neck Pain
Study Overview
Status
Conditions
Detailed Description
Chronic neck pain (CNP) is characterized as persisting pain for more than 3 months, which has a longer expected recovery time. It may be linked to a deficiency or modification of the proprioception of the neck muscles, which is essential for head motor control, cervical joint position, and postural stability (PS). In terms of pain and disability, neck discomfort presents a significant medical problem for patients. According to reports, neck pain is a major cause of illness and a global hardship. The most typical signs of the aforementioned condition are localized, dull, and deep muscle discomfort. Additional symptoms include exhaustion, stiffness, pain, decreased activity, involvement restriction, and difficulty performing coordinated motions.
Standard physiotherapy for persistent neck pain, which includes stretching, isometric exercises, and hot pack therapy, has been shown in recent trials (2021-2024) to effectively reduce pain and improve function. Isometric exercises, self-stretching, active range of motion, heat packs, and self-mobilization methods were all used in this recent randomized controlled experiment.
A breathing technique called diaphragmatic breathing training encourages maximum exhalation, enhances lung ventilation, and facilitates the release of secretions from the trachea. The objectives of these exercises are to modify the recruitment of respiratory muscles, decrease hyperinflation, enhance respiratory muscle function, maximise thoracoabdominal mobility, and lessen dyspnoea. Through diaphragmatic respiration, they can support trunk stability and lung function and posture correction.
CNP is also treated in traditional medicine using various techniques. Electroacupuncture (EA) is one of such techniques; it is safe and doesn't require medication, and numerous studies have shown that it effectively reduces pain and enhances patients' quality of life. Electroacupuncture (EA) is a modified form of acupuncture in which, following a traditional acupuncture procedure, weak electronic currents are applied through the needles.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54782
- University of lahore teaching hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients having a history of the previous 3 months of chronic neck pain
- NPRS 4-7
- Patients having paradoxical breathing
- CVA less than 49 degrees
Exclusion Criteria:
- Congenital abnormality of the cervical spine
- Post-traumatic neck pain
- Hemorrhagic diseases
- Radiculopathy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Physiotherapy care, Diaphragmatic breathing, Electroacupuncture
These patients will receive physiotherapy care, diaphragmatic breathing, and electroacupuncture as part of their treatment program. Total session time: 50 minutes Treatment schedule: 3 sessions on alternate days for 6 weeks |
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Active Comparator: Physiotherapy care, Simple focused breathing, Electroacupuncture
These patients will receive physiotherapy care, simple focused breathing exercises, and electroacupuncture as part of their treatment program. Total session time: 50 minutes Treatment schedule: 3 sessions on alternate days for 6 weeks |
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: Baseline 1st, 3rd and at 6th week of intervention
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Pain intensity will be assessed using the Numeric Pain Rating Scale, an 11 point scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable.
Higher scores indicate greater pain (worse outcome).
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Baseline 1st, 3rd and at 6th week of intervention
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Neck Disability
Time Frame: Baseline 1st, 3rd and at 6th week of intervention
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Neck disability will be assessed using the Neck Disability Index Urdu version , a 10-item questionnaire with a total score ranging from 0 to 50.
Higher scores indicate greater disability (worse outcome).
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Baseline 1st, 3rd and at 6th week of intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Craniovertebral Angle (CVA)
Time Frame: Baseline 1st, 3rd and at 6th week of intervention
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Craniovertebral angle will be measured in degrees (°) using Kinovea software version 0.8.27 (64-bit) from standardized lateral photographs.
The craniovertebral angle is calculated as the angle between a horizontal line passing through the spinous process of C7 and a line joining C7 to the tragus of the ear.
Higher CVA values indicate improved head and neck posture (better outcome), whereas lower values indicate greater forward head posture (worse outcome).
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Baseline 1st, 3rd and at 6th week of intervention
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Sahreen Anwar, PhD, University of Lahore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neurologic Manifestations
- Nervous System Diseases
- Neurobehavioral Manifestations
- Perceptual Disorders
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Agnosia
- Therapeutics
- Complementary Therapies
- Physical Therapy Modalities
- Rehabilitation
- Anesthesia and Analgesia
- Electric Stimulation Therapy
- Combined Modality Therapy
- Anesthesia
- Analgesia
- Acupuncture Therapy
- Transcutaneous Electric Nerve Stimulation
- Electroacupuncture
Other Study ID Numbers
- UOL/IREB/25/12/0036
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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