Thoracic Spine Rotation Stretching and Scapular Retraction in Asthma Patients
Comparative Effects of Thoracic Spine Rotation Stretching and Scapular Retraction on Chest Expansion, Pulmonary Function Test and Dyspnea in Asthma Patients
1 other identifier
interventional
54
1 country
1
Brief 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. 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 17, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 17, 2025
CompletedFirst Submitted
Initial submission to the registry
March 27, 2026
CompletedFirst Posted
Study publicly available on registry
April 2, 2026
CompletedApril 2, 2026
March 1, 2026
8 months
March 27, 2026
March 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
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.
8 Weeks
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.
8 weeks
Secondary Outcomes (1)
Tape measure
8 Weeks
Other Outcomes (1)
Goniometer
8 Weeks
Study Arms (2)
Thoracic Spine Rotation Stretching Group
EXPERIMENTALParticipants 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 8 weeks in individuals with chronic asthma.
Scapular retraction Group
EXPERIMENTALParticipants 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 eight weeks in individuals with chronic asthma.
Interventions
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 eight weeks, using standardized repetitions within a comfortable range of motion.
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 eight weeks in individuals with chronic asthma.
Eligibility Criteria
You may qualify if:
- Age between (18 to 50).
- Confirmed diagnosis of asthma based on clinical guidelines.
- Nonsmoker.
- Chronic asthma.
- Thoracic spine abnormality
You may not qualify if:
- Acute asthma
- Recent exacerbations.
- History of sever cardiopulmonary, musculoskeletal, infectious diseases.
- Any neurological condition.
- Cognitive impairment.
- Any recent injury of spine, shoulder, or rib cage that limit mobility or cause pain.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sehat medical complex hanjerwal
Lahore, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Riffat Malik
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 27, 2026
First Posted
April 2, 2026
Study Start
April 17, 2025
Primary Completion
December 17, 2025
Study Completion
December 17, 2025
Last Updated
April 2, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share