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NCT06407011Completed

Effects of Swedish Massage Prior Circuit Breathing Training on Asthma

Effects of Swedish Massage Prior Circuit Breathing Training on Asthma Control and Respiratory Function in Patients With Asthma

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

The objective of this study was to determine the effects of Swedish massage prior circuit breathing training on asthma control and respiratory function in patients with asthma.

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
6 May 2024
Start date
5 May 2024
Primary completion date
10 Aug 2024
Lead sponsor
Chulalongkorn University
Diseases
Asthma
NCT number
NCT06407011

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 5 May 2024 to the primary completion date, 10 Aug 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Being a patient who has a history of asthma caused by exercise (Exercise-Induced Asthma).
  • In case of a force majeure event that makes it impossible to continue participating in the research, such as injury from an accident or illness, etc.

Other

  • Participating in less than 80 percent of the training sessions (28 times out of 36 times) for the breathing training group and the group that practiced breathing together with massage.
  • Unwillingness to continue participating in the research.

Who the study is looking for

  • Being a male or female patient with asthma who is between 20 and 65 years old.
  • Being a patient who has been diagnosed by a doctor with asthma for at least 6 months.
  • The severity of the disease has been assessed at levels 2 to 4, meaning the volume of air expelled in the first second of breathing quickly and with full force (Forced Expiratory Volume in one second; FEV1) is between 80% and 30% on the date of data collection. This has been certified by a doctor, and the patient is using medication according to the normal treatment plan.
  • Must not have other respiratory diseases such as tuberculosis, lung cancer, emphysema, chronic obstructive pulmonary disease (COPD), etc.
  • Should not have received exercise training for more than 20 minutes at a time, 3 days/week, or more in the past 6 months before participating in the research.
  • Having no communication problems.
  • The sample volunteers to participate in the research and agrees to sign the consent form to participate in the research.

Age in the registry: 20 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Sports Science, Chulalongkorn University
Coordinator of this site? Confirm its status
Pathum WanThailandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.