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Effects of Cervical Spine Retraction Exercise With and Without Diaphragmatic Breathing in Forward Head Posture.

Not Applicable
Recruiting
Conditions
Forward Head Posture
Interventions
Other: Cervical Retraction Exercise
Other: Diaphragmatic Breathing
Other: Baseline Treatment
Registration Number
NCT06130969
Lead Sponsor
Riphah International University
Brief Summary

This study aims to determine the effect of combining diaphragmatic exercises with cervical retraction exercise on pain, disability, active range of motions of cervical spine and craniovertebral angle in individuals with forward head posture.

Detailed Description

Forward head posture altering breathing pattern is one of the most common musculoskeletal deformity. Diaphragmatic exercises can reduce pain and disability levels, and correct forward head posture (FHP) in patients with neck discomfort.

In this randomized clinical trial, fifty two participants displaying forward head posture (FHP) will be randomly assigned to one of the two intervention groups: the Diaphragmatic Exercises and Cervical Retraction Exercise Combined Group or the Cervical Retraction Exercise Alone Group. Randomization will be performed using a convenient random sampling method via sealed opaque envelopes. Each participant will receive a total of twelve treatment sessions over a four-week period. The efficacy of the interventions will be assessed at the beginning (first session), conclusion (twelfth session), and two weeks after completing the sessions. Outcome measures, including pain intensity, disability levels, cervical range of motion, and craniovertebral angle (CVA), will be evaluated using the Numeric Pain Rating Scale (NPRS), Neck Disability Index (NDI), universal goniometer and Image J software, respectively. Data will be analyzed using Statistical Package for the Social Sciences (SPSS) software version 26. Normality of data will be assessed using the Kolmogorov-Smirnov test. For within-group comparisons, either repeated measures ANOVA or the Friedman test will be used. To compare changes between the groups, the independent t-test or Mann-Whitney U test will be applied, depending on the data distribution. The analysis of these outcome measures will provide valuable insights into the impact of the interventions on participants' symptoms and postural alignment.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Primary complaint of neck pain (pain on the posterior part of the cervical spine to the beginning of the thoracic area with or without pain in the shoulder girdle)
  • Age from 20 to 35 years
  • Both gender
  • CVA <49° (16)
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Exclusion Criteria
  • Any serious pathology such as tumor
  • Had history of whiplash injury within 3 months of the examination,
  • Underwent prior surgery to the cervical spine
  • Currently using muscle relaxation medication.
  • Degenerative conditions
  • Exhibited positive neurologic signs consistent with nerve root compression.
  • Patients with a history of respiratory disease, such as repeated bronchitis, pneumonia, asthma, pulmonary lymph nodes, pleurisy, cured tuberculosis and others
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group BCervical Retraction ExerciseCervical Retraction exercise with diaphragmatic breathing along with baseline treatment
Group BBaseline TreatmentCervical Retraction exercise with diaphragmatic breathing along with baseline treatment
Group ACervical Retraction ExerciseCervical Retraction exercise without diaphragmatic breathing along with baseline treatment
Group BDiaphragmatic BreathingCervical Retraction exercise with diaphragmatic breathing along with baseline treatment
Group ABaseline TreatmentCervical Retraction exercise without diaphragmatic breathing along with baseline treatment
Primary Outcome Measures
NameTimeMethod
Numeric pain rating scale (NPRS):6 weeks

The NPRS is a subjective pain rating scale using an 11-point scale from 0 to 10, where 0 means 'no pain' and 10 means 'intolerable pain'. Participants select the whole number that best represents their level of pain.

Goniometer for Cervical Range of motion (CROM)6 weeks

Universal goniometer has fair inter-tester reliability ranging from 0.79-0.92. Validity of this tool is good i.e. 0.97-0.98 This tool is most commonly used in the clinical settings for evaluating joint ROM.

Photogrammetry for Craniovertebral Angle (CVA) by image j software6 weeks

CVA, can be measured using the lateral photos exposing C7 and the ear. The participants will maintain the natural head posture through the measurement method of self-balance posture. It is the angle made by the line that connects the seventh cervical spine with the tragus and the horizontal line of the seventh cervical spine in the sitting and standing positions. A CVA of \<49° is characterized as FHP (3).

Image J is an image processing and analysis program that can read both image file formats and raw formats. It can display, edit, analyze, process, store, and print images, as well as measure distances and angles.

Neck disability index (NDI):6 weeks

that restricts the activities of daily living (ADL); it also helps to determine self- assessed disability. NDI has 10 domains covering pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation. Scores range from 0 to 50, with 50 being the greatest levels of dysfunction.

Secondary Outcome Measures
NameTimeMethod
Global rating of change (GRC)6 weeks

GRC scale is used as an objective means to test the improvement of patient symptoms, to identify the intervention effect after treatment completion in clinical practice

Trial Locations

Locations (1)

Chiropractor & Physio Pain Relief Center

🇵🇰

Lahore, Punjab, Pakistan

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