CompletedPhase 2ACTRN12606000449538

The effect of spinal manipulation on respiratory function - a pilot study

The effect of combining spinal manipulation with exercise on the respiratory function of normal individuals


Sponsor

Roger Engel

Enrollment

50 participants

Start Date

Mar 1, 2005

Study Type

Interventional

Conditions

Summary

Respiratory function involves movement of structures related to the Cervical and Thoracic spines. Evidence exists that the application of spinal manipulation to these areas can alter respiratory function. This study tests the effect administering spinal manipulation with exercise has on the respiratory function of normal individuals. The aim is to develop a pulmonary rehabilitation protocol that includes spinal manipulation for use in the management of chronic respiratory disease.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 40 Yearss

Plain Language Summary

Simplified for easier understanding

This pilot study examines whether spinal manipulation affects breathing function in healthy adults. Non-smokers ages 18 to 40 without respiratory disease participate in spinal manipulation sessions while researchers measure changes in lung function.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

This trial measures the effect of administering spinal manipulation with and without exercise on the respiratory function of normal individuals. Participants with lung volume measurements at the lower

This trial measures the effect of administering spinal manipulation with and without exercise on the respiratory function of normal individuals. Participants with lung volume measurements at the lower end of the normal range are allocated to 4 experimental groups. Group 1 receives exercise only; Group 2 receives spinal manipulation only; Group 3 receives spinal manipulation & exercise; Group 4 receives no intervention (Control). Each participant receives 6 intervention sessions over a 4 week period.


Locations(1)

Australia

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ACTRN12606000449538