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An intervention study of combined exercise in a normobaric hypoxic environment in overweight and obese young women

An intervention study of combined exercise in a normobaric hypoxic environment in overweight and obese young women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091730
Enrollment
Unknown
Registered
2024-11-01
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

overweight and obesity

Interventions

Normal Pressure Oxygen Combination Exercise Set:Combined exercise interventions in normobaric and normoxic environments
Normal Pressure Low Oxygen Combination Exercise Set:Combined exercise interventions in a normobaric low-oxygen environment (oxygen concentration of about 15%, altitude of 2500 meters)

Sponsors

Beijing Xiaotangshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 44 Years

Inclusion criteria

Inclusion criteria: ? Females aged =18 and <45 years; ? BMI is: =24 and <32.5; ?Capable of completing cardiopulmonary exercise test (subject to clinician's judgment); ? Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: ? History of musculoskeletal trauma and acute illness within the last 1 month; ? Those who have a regular exercise habit lasting more than 6 months before the intervention; ? Those who are participating in other weight reduction related trials; ? People with acute plateau reaction; ? People with cardiovascular and cerebrovascular diseases such as tertiary hypertension, arrhythmia and coronary heart disease; (6) Diabetes mellitus that is not effectively controlled ? People with respiratory diseases such as asthma; ? people taking weight control drugs (e.g. orlistat, lipstatin, phentermine, bupropion, etc.); ?High-altitude residents, who had been exposed to low oxygen at an altitude of more than 1500m in the 6 months prior to the intervention; ?Pregnant and lactating women; ?Considered by the investigator to be unsuitable for participation in the trial.

Design outcomes

Primary

MeasureTime frame
body mass index;

Secondary

MeasureTime frame
body composition;body circumference;cardiopulmonary function;Blood-related indicators;intestinal flora;

Countries

China

Contacts

Public ContactSun Jie

Beijing Xiaotangshan Hospital

bingxuehaitun520@163.com+86 134 8866 5637

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026