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Asthma ChronicNCT07508267

Thoracic Spine Rotation Stretching and Scapular Retraction in Asthma Patients

A study testing Thoracic Spine Rotation Stretching and Scapular retraction in people with Asthma Chronic, run by Riphah International University at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Patients with asthma frequently experience upper back stiffness and rounded shoulders and tightness in the thoracic region. Rib cage stiffness occurs due to poor posture and muscle tightness, which leads to decreased chest expansion and increased use of accessory muscles during breathing. Read more about this study

Who is it for?
Ages 18 to 50 years
Conditions the study is for
Asthma Chronic
What is being tested?
Thoracic Spine Rotation Stretching and Scapular retraction
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 sitePakistan
Study dates
17 Apr 2025to 17 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age between (18 to 50).
  • Confirmed diagnosis of asthma based on clinical guidelines.
  • Nonsmoker.
  • Chronic asthma.
  • Thoracic spine abnormality

Who cannot join

  • Acute asthma
  • Recent exacerbations.
  • History of severe cardiopulmonary, musculoskeletal, infectious diseases.
  • Any neurological condition.
  • Cognitive impairment.
  • Any recent injury of spine, shoulder, or rib cage that limit mobility or cause pain.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Sehat medical complex hanjerwal

    Lahore

Other trials in Pakistan

About this study

Official title: Comparative Effects of Thoracic Spine Rotation Stretching and Scapular Retraction on Chest Expansion, Pulmonary Function Test and Dyspnea in Asthma Patients

Patients with asthma frequently experience upper back stiffness and rounded shoulders and tightness in the thoracic region. Rib cage stiffness occurs due to poor posture and muscle tightness, which leads to decreased chest expansion and increased use of accessory muscles during breathing. Additionally, rounded shoulders can hinder proper opening of the chest, preventing the lungs from expanding properly. Thoracic spine rotation stretching targets the thoracic paraspinal muscles, erector spinae, and intercostal muscles. This exercise helps improve thoracic mobility, increases chest expansion and pulmonary function, and reduces dyspnea. The other exercise is Scapular Retraction, which targets the rhomboids, trapezius, and posterior deltoids that help in chest opening and lead to chest expansion and allow lungs to expand more fully during inhalation. Together, these exercises improve chest expansion and pulmonary function, reduce dyspnea, and improve posture.

Read the detailed description

Asthma is a prevalent chronic respiratory condition that affects millions worldwide, characterized by airway inflammation and reversible airflow obstruction. Patients often experience difficulty in breathing, which can severely impact their quality of life. People with asthma are less active that their peers, and consequently, the patient becomes more sedentary. This study focusses to compare the effects of thoracic spine rotation stretching and Scapular Retraction exercises on chest expansion, pulmonary function, and dyspnea in patients with asthma. By investigating these interventions, the study seeks to provide practical recommendations for enhancing the management of asthma symptoms, ultimately improving respiratory function and mobility may improve asthma control and quality of life.

A randomized clinical trial will enroll participants aged 18 to 50 with a confirmed diagnosis of chronic asthma. The study will take place at Rai Medical College Teaching Hospital Sargodha, utilizing a non- probability convenient sampling technique for participant selection. Participants will be randomly assigned to two groups using a lottery method, ensures a diverse yet unbiased sample. Group A will perform thoracic spine rotation stretching, while Group B will engage in Scapular Retraction exercises, following a standardized warm-up. Baseline treatment will include breathing exercises, postural education, bronchodilators, and nebulization Each group will engage in their respective exercises for a defined duration, focusing on improving respiratory mechanics and muscle flexibility. Study will be completed in 4 weeks (3x/week). After data collection, data will be analyzed using SPSS version 26. Assessments will be conducted before and after the intervention period, measuring chest expansion with a measuring tape, pulmonary function through digital spirometer (including FEV1 and FVC their ratio and peak expiratory flow), and dyspnea levels using the Modified borg dyspnea scale, thoracic rotation range of motion measured with a goniometer. The integration of targeted physical therapy in this study has the potential to significantly improve asthma management by enhancing respiratory function, reducing dyspnea, and increasing chest expansion.

Conditions
Asthma Chronic
Being tested
Thoracic Spine Rotation Stretching, Scapular retraction
Keywords
Asthma, Chest Expansion, Dyspnea, Pulmonary Function, Scapular Retraction, Thoracic Spine Rotation
Medical subject headings
Asthma, Dyspnea

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Thoracic Spine Rotation StretchingOther

    Thoracic spine rotation stretching consists of controlled rotational movements of the thoracic spine performed to improve thoracic mobility. The exercises are administered under supervision, three sessions per week for four weeks, using standardized repetitions within a comfortable range of motion.

  • Scapular retractionOther

    Scapular retraction exercises involve active scapular retraction movements performed to improve shoulder and upper thoracic mobility. The intervention is administered under supervision, three sessions per week for four weeks in individuals with chronic asthma.

Study groups in NCT07508267
Study groupRoleWhat they receive
Thoracic Spine Rotation Stretching GroupExperimentalParticipants will undergo thoracic spine rotation stretching exercises to assess their effects on pulmonary function, chest expansion, and dyspnea and also improve thoracic rotation . The intervention will be provided 3 sessions per week for a duration of four weeks in individuals with chronic asthma.
Receives: Other: Thoracic Spine Rotation Stretching
Scapular retraction GroupExperimentalParticipants will perform Scapular Retraction exercises to evaluate their effects on pulmonary function, chest expansion, and dyspnea. The intervention will be provided three sessions per week for a duration of four weeks in individuals with chronic asthma.
Receives: Other: Scapular retraction

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Modified borg scale

    Dyspnea at rest was assessed using the modified Borg scale. It is a well-validated scoring system using a 0-to-10-point scale.The intensity of dyspnea is most often assessed according to a symptom scale, with the modified Borg scale, which measures dyspnea on a scale of 0-10 arbitrary units, being used most frequently.It is a validated dyspnea scale ranging from 0 ("no shortness of breath") to 10 ("worst shortness of breath") points.

    Measured: 4 Weeks

  2. Digital spirometer:

    A digital spirometer will be used to measure pulmonary function tests including FEV1, FVC, FEV1/FVC.The normal values of FEV1/FVC ratio are >0.70 and FVC, FEV1 are >80% or predicted age.

    Measured: 4 weeks

Secondary outcomes (1)
  1. Tape measure

    Chest expansion was measured using a measurement tape (Baseline 12-1201 with Gulick attachment, Fabrication Enterprises Inc., New York, NY, USA) to determine the difference between rib cage circumference at the end of forced expiration and rib cage circumference at the end of forced inspiration. Chest expansion measurement is highly reliable with an interexaminer intraclass correlation coefficient of 0.99.The chest circumference was measured in cm at maximum inspiration and maximum expiration by horizontally passing through the junction of the xiphoid process and the body of the sternum so that the chest girth was exposed.The tape measure is wrapped around the thorax in a level position and pulled just taut (but not restricting chest expansion) at three anatomic sites.1. The angle of Louis on the sternum .2.The xiphoid process for mid-chest expansion 3.The midpoint between the xiphoid process and the umbilicus for lower chest expansion, where most of the bucket handle motion occur.

    Measured: 4 Weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Apr 2026
  2. Study start17 Apr 2025
  3. Primary completion17 Dec 2025
  4. Study completion17 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07508267
Sponsor's protocol ID
Mehwish Atta
Status last verified
Sep 2026
First submitted
27 Mar 2026
Last updated
28 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Thoracic Spine Rotation Stretching and Scapular retraction in people with Asthma Chronic, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Modified borg scale (time frame: 4 Weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Sep 2026.

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