- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07802080
Effects of Kettlebell Swing Training Combined With Breathing Exercises on Respiratory Muscle Strength and Pulmonary Function in Overweight and Obese Young Adults (Kettlebell)
Overweight and obesity are associated with impaired breathing mechanics, including reduced chest wall and diaphragmatic movement, decreased respiratory muscle strength and endurance, and inefficient breathing patterns. These changes may adversely affect pulmonary function, autonomic regulation, and physical capacity.
This study aims to compare the effects of kettlebell swing exercise combined with breathing training versus breathing training alone in individuals with overweight or obesity. Outcomes will include respiratory muscle strength, pulmonary function, heart rate variability, and body composition. The findings may help determine whether adding kettlebell swing exercise to breathing training provides additional benefits for respiratory and cardiometabolic health in this population.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
A total of 40 young adults aged 18-25 years with overweight or obesity (body mass index [BMI] ≥23.0 kg/m²) will be recruited and randomly assigned to one of two groups.
The experimental group will perform kettlebell swing exercise combined with breathing training for 40 minutes per session. The control group will receive breathing training alone for 20 minutes per session. Both groups will participate in their assigned intervention three times per week for 6 weeks.
Outcome measures will include respiratory muscle strength, pulmonary function, heart rate variability (HRV), and body composition.
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Pacharee Manoy, Ph.D.
- Telefonnummer: Thailand: +66 (54) 466 697
- E-post: pachareeman@gmail.com
Studer Kontakt Backup
- Navn: Patchareeya Amput, Ph.D.
- Telefonnummer: Thailand: +66 (54) 466 697
- E-post: patchareeya.am@up.ac.th
Studiesteder
-
-
Changwat Phayao
-
Phayao, Changwat Phayao, Thailand, 56000
- Rekruttering
- School of Allied Health Sciences, University of Phayao
-
Ta kontakt med:
- Pacharee Manoy, Ph.D.
- Telefonnummer: 3339 Thailand: +66 (54) 466 666
- E-post: pacharee.ma@up.ac.th
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Male or female adults aged 18-25 years with a body mass index (BMI) of ≥23.0 kg/m².
- Individuals who are physically inactive or sedentary, defined as exercising fewer than 3 days per week or engaging in less than 150 minutes of exercise per week.
- Willingness to provide written informed consent to participate in the study.
Exclusion Criteria:
- Presence of bodily pain, particularly in the upper or lower extremities, with a Visual Analogue Scale (VAS) score of >3/10.
- Musculoskeletal disorders, such as scoliosis.
- History of neurological disorders, including spinal cord injury, epilepsy, or stroke.
- History of respiratory or cardiovascular diseases, including hypertension, heart disease, emphysema, asthma, previous lung lobectomy, or lung cancer.
- History of chronic non-communicable diseases or other systemic disorders, including diabetes mellitus, kidney disease, liver disease, endocrine disorders, or immune system disorders.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Experimental group
Kettlebell swing training combined with breathing exercises
|
Kettlebell swing training combined with breathing exercises, performed three times per week for 40 minutes per session over 6 weeks.
|
|
Sham-komparator: Control group
Breathing exercises
|
Breathing exercises performed three times per week for 20 minutes per session over 6 weeks.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Repiratory muscle strength
Tidsramme: Before and after the 6 week intervention
|
Respiratory muscle strength will be measured using a handheld manometer (MicroRPM).
Participants will be instructed to perform a maximal inspiratory effort from residual volume to assess maximal inspiratory pressure (PImax) and a maximal expiratory effort from total lung capacity to assess maximal expiratory pressure (PEmax).
|
Before and after the 6 week intervention
|
|
Heart rate variability (HRV)
Tidsramme: Before and after the 6 week intervention
|
Time and frequency-domain heart rate variability (HRV) parameters will be measured using the SA-3000P analyzer.
|
Before and after the 6 week intervention
|
|
Pulmonary function test
Tidsramme: Before and after the 6 week intervention
|
Vital capacity (VC), expiratory reserve volume (ERV), forced vital capacity (FVC), forced expiratory volume in 1 second (FEV₁), and the FEV₁/FVC ratio will be measured using a portable spirometer.
|
Before and after the 6 week intervention
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Body composition
Tidsramme: Before and after the 6 week intervention
|
Muscle mass and fat mass will be assessed using bioelectrical impedance analysis (BIA).
|
Before and after the 6 week intervention
|
Samarbeidspartnere og etterforskere
Sponsor
Publikasjoner og nyttige lenker
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- HREC-UP-HSST 1.2/111/69
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .