ClinicalTrials.gg
Active, not recruitingNCT07752420Updated Oct 13, 2026

Effects of Structural Integration on Chest Wall Expansion Among COPD Patients

An interventional study of Structural Integration with Conventional Pulmonary Rehabilitation and Pulmonary Rehabilitation only in COPD (With - Without Rehabilitation), sponsored by Green International University. Active, not recruiting at 1 site in Pakistan. Open to participants aged 50 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Green International University · Not applicable, Interventional, and Supportive care

Updated Oct 13, 2026Now Active, not recruitingGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
50 Years to 70 Years
Sex
All
01

Study summary

The present study aims to investigate the effects of the 10-Series of Structural Integration on chest wall expansion in patients with stable COPD using a randomized controlled trial design. Participants receiving Structural Integration in addition to conventional pulmonary rehabilitation will be compared with those receiving conventional pulmonary rehabilitation alone. Chest wall expansion will serve as the primary outcome, while pulmonary function, dyspnea, functional exercise capacity, and quality of life may be evaluated as secondary outcomes.

02

Conditions studied

  • COPD (With - Without Rehabilitation)

Keywords

  • COPD
  • Structural Integration
  • Chest Wall Expansion
  • Pulmonary Rehabilitation
03

In context

Pulmonary Disease, Chronic Obstructive

5,520 studies on the registry are indexed under Pulmonary Disease, Chronic Obstructive; 856 are open to participants now.

This study's planned enrollment of 52 is below the median of 62 across 3,839 interventional studies indexed under Pulmonary Disease, Chronic Obstructive.

Browse Pulmonary Disease, Chronic Obstructive studies →

Lead sponsor

Green International University is the lead sponsor of 17 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Clinically diagnosed stable according to GOLD criteria
  • GOLD stage II or III
  • No acute exacerbation within the previous four weeks
  • Able to ambulate independently
  • Medically cleared to participate in pulmonary rehabilitation
  • Willing to provide written

Exclusion criteria

Exclusion Criteria:

  • Severe cardiovascular disease contraindicating exercise
  • Recent thoracic or abdominal surgery (\<6 months)
  • Rib fractures or severe chest wall deformity
  • Neurological disorders affecting mobility
  • Active
  • Severe osteoporosis with high fracture risk
  • Previous Structural Integration treatment within the last year
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
52 participants (estimated)

Study arms

  • Experimental
    Experimental Group

    Other: Structural Integration with Conventional Pulmonary Rehabilitation

  • Active comparator
    Control Group

    Other: Pulmonary Rehabilitation only

Interventions

  • OtherStructural Integration with Conventional Pulmonary Rehabilitation

    * Conventional pulmonary rehabilitation. * The complete 10-Series of Structural Integration, delivered by a certified Structural Integration practitioner/physiotherapist.

  • OtherPulmonary Rehabilitation only

    Participants receive only the conventional pulmonary rehabilitation program.

06

What researchers measure

Primary outcomes

  1. Chest Wall Expansion

    Chest wall expansion will be measured using a flexible measuring tape at: * Axillary level * Xiphoid level * Lower thoracic level (10th rib) Measurements will be taken during maximal inspiration and maximal expiration. The difference (in centimeters) will be recorded. Three readings will be obtained at each level, and the average value will be used for analysis.

    Time frame: Before the start and end of 10 weeks

07

Study locations

1 site
  • Ali Fatima Hospital
    Lahore, Punjab Province 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: Yes — The details will be provided to researchers subject to reason of IPD requirement. The record will be provided through Email. Only official Emails will be entertained.

Supporting information: Study protocol, Clinical study report

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Active, not recruiting
changed Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    Not yet recruiting→Active, not recruiting
    + 3 other changes: verification date, date precision and contact details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07752420
Lead sponsor
Green International University
Responsible party
Mohtishim Ahmed (Assistant Professor, Green International University) — Principal investigator
First posted
Aug 7, 2026
Start date
Sep 1, 2026
Primary completion
Nov 15, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Oct 13, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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