Effects of Structural Integration on Chest Wall Expansion Among COPD Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-70
SponsorGreen International University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Clinically diagnosed stable COPD according to GOLD criteria

GOLD stage II or III

No acute exacerbation within the previous four weeks

Able to ambulate independently

Disqualifiers

Severe cardiovascular disease contraindicating exercise

Recent thoracic or abdominal surgery (<6 months)

Rib fractures or severe chest wall deformity

Neurological disorders affecting mobility

Trial design

Design model

Parallel

Treatments tested in this trial

  • Structural Integration with Conventional Pulmonary Rehabilitation

    Other intervention

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

  • Pulmonary Rehabilitation only

    Other intervention

    Participants receive only the conventional pulmonary rehabilitation program.

Treatment groups

52 Participants
are divided into 2 treatment groups
Group A: Experimental GroupExperimental treatment 1 intervention
Group B: Control GroupActive comparator 1 intervention

Trial outcomes

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

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: