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Not yet recruiting

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

Biruni University

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

NCT IDNCT07663591
Org study ID2026ML

Timeline

Milestones

Study first posted2026-06-23actual
Last update posted2026-06-23actual
Study start2026-07-01estimated
Primary completion2026-07-01estimated
Study completion2026-07-30estimated

Assets

Investigational agents

Who this study enrolls

Obesity / overweight

Who can enroll

Minimum age25 Years
Maximum age60 Years
SexAll
Healthy volunteersAccepted
Sampling methodNon probability sample

Study population text

Individuals with obesity using incretin based therapy

Inclusion criteria

Individuals aged 25-60 years
Individuals with a body mass index (BMI) ≥ 30 kg/m² according to the World - Health Organization (WHO) classification of obesity
Individuals who voluntarily agree to participate in the study

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

Other (unclassified)
15
Weight & body composition
3
Glycemic / diabetes
1
Cardiometabolic biomarkers
1

Weight & body composition

3 endpoints
Secondary/protocol endpoint

Waist Index (WI) Adjusted for Weight

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint

Body fat mass

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint

Waist circumference

Time frame:Baseline to 3 months

descriptive

Glycemic / diabetes

1 endpoint
Secondary/protocol endpoint

Fasting plasma glucose (FPG) and glycosylated hemoglobin (HbA1c)

Time frame:Baseline to 3 months

concentration, descriptive

Cardiometabolic biomarkers

1 endpoint
Secondary/protocol endpoint

Lipid profile

Time frame:Baseline to 3 months

descriptive

Other (unclassified)

15 endpoints
Primary/protocol endpoint/low confidence

Maximum Inspiratory Pressure (MIP)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Maximum Expiratory Pressure (MEP)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Forced vital capacity (FVC)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Forced expiratory volume in the first second (FEV1)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

FEV1/FVC

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Respiratory Muscle Endurance

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Functional capacity

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Ventilation (VE)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Peak respiratory reserve (BRpeak)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Peak ventilation (VEpeak)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Inspiratory capacity (IC)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Skeletal Muscle Mass Index (SMMI)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Body Roundness Index (BRI)

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Body muscle mass

Time frame:Baseline to 3 months

descriptive

Secondary/protocol endpoint/low confidence

Daily step count

Time frame:Baseline to 3 months

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 6, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.