Clinical Trial

Laser Acupuncture for Pulmonary Function Test and Quality of Life in COPD Patients

Completed
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Summary
This clinical trial aims to evaluate the effectiveness and safety of laser acupuncture as an adjunct therapy in patients with chronic obstructive pulmonary disease (COPD). The main research questions are: * Does laser acupuncture, when combined with standard pharmacological treatment, improve lung function (measured by FEV1% and FEV1/FVC ratio) more than sham laser acupuncture after 4 weeks of therapy? * Does this combination also lead to better quality of life, as assessed by the COPD Assessment Test (CAT) and the St. George's Respiratory Questionnaire (SGRQ), compared to the control group, after 4 and 8 weeks? * Is there a correlation between lung function (FEV1%) and quality of life scores (CAT and SGRQ)? * Are there any significant adverse effects caused by laser acupuncture compared to sham treatment? Participants will: * Undergo spirometry and complete CAT and SGRQ questionnaires. * Receive either laser acupuncture or sham laser acupuncture sessions. * Return for follow-up assessments at 4 and 8 weeks.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-06-12; most recent amendment 2025-12-30.
Status change: Recruiting → Completed 2025-12-30
Status change: Not Yet Recruiting → Recruiting 2025-08-06
Trial Details
NCT Number NCT07030452
Lead Sponsor Indonesia University
Conditions Chronic Pulmonary Obstruction
Enrollment 40 participants
Start Date 2025-08-01
Primary Completion 2025-12-10 (estimated)
Study Completion 2025-12-10 (estimated)
Updated on ClinicalTrials.gov 2025-12-31