Machine Learning Prediction of Respiratory Muscle Changes and Ventilatory Responses After Incretin-Based Therapy in Obesity
Prediction of Changes in Pulmonary Function, Respiratory Muscle Performance, and Ventilatory Responses Following Incretin-Based Therapy in Individuals With Obesity Using Machine Learning
Lead sponsor
Asset
GLP-1 / incretin class catch-all
Listed sites
0
Recruiting sites
-
Estimated enrollment
48
Study population
Obesity / overweight
Eligibility highlights
•BMI ≥30
Primary endpoint
•Maximum Inspiratory Pressure (MIP)
Registered trial locations
Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Who this study enrolls
Who can enroll
Study population text
Individuals with obesity using incretin based therapy
Inclusion criteria
Exclusion criteria
Charlson Comorbidity Index (CCI) score ≥ 3 Uncontrolled arrhythmia, hypertension, heart failure, diabetes mellitus, or unstable angina pectoris Cognitive, orthopedic, or neurological conditions that may interfere with study assessments or treatment procedures History of lower extremity injury or surgery within the previous 6 months Diagnosis of diabetes mellitus with complications such as nephropathy, retinopathy, or neuropathy Presence of chronic respiratory disease Acute infection at the time of assessment Middle ear pathologies (e.g., tympanic membrane rupture or otitis) History of spontaneous or traumatic pneumothorax Current smoking Pregnancy STOP-Bang score ≥ 3 Participation in a structured weight-loss diet program or receipt of medical treatment for weight reduction during the assessment period History of endoscopic weight-loss procedures and/or bariatric surgery within the previous 12 months
Endpoints (20)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Weight & body composition
3 endpointsWaist Index (WI) Adjusted for Weight
Time frame:Baseline to 3 months
descriptive
Body fat mass
Time frame:Baseline to 3 months
descriptive
Waist circumference
Time frame:Baseline to 3 months
descriptive
Glycemic / diabetes
1 endpointFasting plasma glucose (FPG) and glycosylated hemoglobin (HbA1c)
Time frame:Baseline to 3 months
concentration, descriptive
Cardiometabolic biomarkers
1 endpointLipid profile
Time frame:Baseline to 3 months
descriptive
Other (unclassified)
15 endpointsMaximum Inspiratory Pressure (MIP)
Time frame:Baseline to 3 months
descriptive
Maximum Expiratory Pressure (MEP)
Time frame:Baseline to 3 months
descriptive
Forced vital capacity (FVC)
Time frame:Baseline to 3 months
descriptive
Forced expiratory volume in the first second (FEV1)
Time frame:Baseline to 3 months
descriptive
FEV1/FVC
Time frame:Baseline to 3 months
descriptive
Respiratory Muscle Endurance
Time frame:Baseline to 3 months
descriptive
Functional capacity
Time frame:Baseline to 3 months
descriptive
Ventilation (VE)
Time frame:Baseline to 3 months
descriptive
Peak respiratory reserve (BRpeak)
Time frame:Baseline to 3 months
descriptive
Peak ventilation (VEpeak)
Time frame:Baseline to 3 months
descriptive
Inspiratory capacity (IC)
Time frame:Baseline to 3 months
descriptive
Skeletal Muscle Mass Index (SMMI)
Time frame:Baseline to 3 months
descriptive
Body Roundness Index (BRI)
Time frame:Baseline to 3 months
descriptive
Body muscle mass
Time frame:Baseline to 3 months
descriptive
Daily step count
Time frame:Baseline to 3 months
descriptive
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 6, 2026 snapshot.