Low Volume Nose Breathing Exercises With an Incentive Spirometer for Cervical Spinal Cord Injury Patients
Official title: Effect of Low Volume Nose Resistance Breathing Exercise With Incentive Spirometer on Pulmonary Function Test, Dyspnea, Cough and Sputum in Patient With Cervical Spinal Cord Injuries
Run by Riphah International University · NCT07645027 · Data updated 2026-11-12
This trial tests whether adding low-volume nose resistance breathing with an incentive spirometer to standard respiratory therapy helps people with cervical spinal cord injury breathe better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 38 Years |
| Sex | All |
| Enrollment | 42 (estimated) |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Status | Recruiting |
| Started | May 1, 2026 |
| Main results expected | August 1, 2026 |
| Study ends | August 1, 2026 |
| Registry record updated | June 12, 2026 |
| Trial ID | NCT07645027 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are inpatients aged 18–38 with recent cervical SCI (C4–C7), within one year of injury, able to consent, and without severe pulmonary disease.
✕Probably not a fit
Patients with longer-standing injury, severe comorbidities, or contraindications to pulmonary interventions may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares two respiratory rehabilitation strategies for adults with cervical spinal cord injury (C4–C7) in inpatient rehab. Group A receives low-volume nose resistance breathing exercises using an Acapella device plus incentive spirometry for 20 minutes, three times daily, five days a week, over four weeks; Group B receives conventional respiratory physiotherapy with the same frequency and duration. Outcomes include pulmonary function test results, dyspnea, cough effectiveness, and sputum characteristics, measured before and after the intervention. Statistical analyses will assess intra- and intergroup differences, with a significance level of p < 0.05. The study aims to determine if the LVNRBE plus IS approach provides added benefits over standard therapy in this population.
Why it matters
Potential benefit: If successful, patients may experience improved lung function, reduced dyspnea, and better airway clearance.
How similar studies have gone: Previous pulmonary rehabilitation efforts with breathing exercises and incentive devices have shown respiratory benefits in similar populations, but this specific LVNRBE plus IS combination is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagonosed cervical spine injury C4-C7 * Age 18-38 years * Undergoing in-patient rehabilitation * No previous history of severe pulmonary disease * Disease duration \<1 year * Ability to give informed consent * Road Accident Exclusion Criteria: * Uncontrolled hypertension * Other Neuromuscular disease * Stage 3-4 pressure wound * Clinical instability * Traumatic Brain injury
Where it's running
-
Jinnah hoapital
Lahore, Punjab Province, Pakistan Recruiting
Study contacts
- Principal investigator: Arjumand Bano, MS — Riphah International University
- Study coordinator: Muhammad Iqbal Tariq, Phd
- Email: iqbal.tariq@riphah.edu.pk
- Phone: 333826752
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.