Skip to main content
Clinical Trials/CTRI/2025/07/090423
CTRI/2025/07/090423Not yet recruitingNot Applicable

Effect of Diaphragmatic Stretching on Cardiopulmonary Parameter in Post Pulmonary TB Sequalae Patient

Delhi Pharmaceutical Sciences and Research University1 site in 1 country40 target enrollmentStarted: July 21, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
a) PEFR (peak expiratory flow rate) (l/min)

Study Overview

Brief Summary

This study investigates the effect of diaphragmatic stretching on cardiopulmonary parameters in patients with post tuberculosis lung sequelae. The primary aim is to evaluate whether diaphragmatic stretching can improve respiratory functions such as PEFR chest expansion and other cardiopulmonary measures in these patients potentially aiding in respiratory rehabilitation and management of post TB lung damage.

Study Design

Study Type
Interventional
Allocation
Other
Masking
Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 55.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Subjects with post pulmonary TB sequalae who are diagnosed and referred by the pulmonologist or physician.
  • 2.Both the gender will be included 3.Subject who has Completed course of ATT.
  • 4.Subject with sputum smear as well as culture negative.
  • X-Ray finding show no active infection finding.

Exclusion Criteria

  • 1.Patient with multi drug resistant TB.
  • 2.Life threating disorder.
  • 3.History of recent cardiothoracic or abdominal surgery.
  • 4.Acute rib fracture.
  • 5.History of psychiatric illness.
  • • Recent history of chest wall or abdominal trauma.
  • • History of any other neurological, psychological, systemic, musculoskeletal disorder that can interfere with the rehabilitation programme or can affect the outcome of the study.

Outcomes

Primary Outcomes

a) PEFR (peak expiratory flow rate) (l/min)

Time Frame: pre- before intervention | post - after intervention on the same day

b) Resting Heart rate (bpm)

Time Frame: pre- before intervention | post - after intervention on the same day

c) chest expansion (cm)

Time Frame: pre- before intervention | post - after intervention on the same day

d) Oxygen saturation(Spo2)

Time Frame: pre- before intervention | post - after intervention on the same day

Secondary Outcomes

  • a) Resting blood pressure (mmhg)(pre- before intervention)

Investigators

Sponsor
Delhi Pharmaceutical Sciences and Research University
Sponsor Class
Research institution
Responsible Party
Principal Investigator
Principal Investigator

Minal Fiza

Delhi Pharmaceutical Sciences and Research University

Study Sites (1)

Loading locations...

Similar Trials