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EXISECRET

UnknownPhase NA

Exercise and GLP-1 RA on Insulin Secretion

Effects of 12 Weeks of Endurance Exercise Training Alone or in Combination With Glucagon Like Peptide 1 Receptor Agonist (GLP-1 RA) Treatment on Insulin Secretory Capacity in Type 2 Diabetes

Asset

Semaglutide

GLP-1 agonist

Listed sites

1

Recruiting sites

1

Enrollment

30

estimated

Study population

Obesity / overweight, Type 2 diabetes

Key I/E criterion

BMI 28-35

Primary endpoint

Insulin secretion

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT04383197
Org study IDH-19008233

Timeline

Milestones

Study start2019-12-10actual
Study first posted2020-05-12actual
Last update posted2021-02-11actual
Primary completion2021-08estimated (month precision)
Study completion2022-08estimated (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweightType 2 diabetes

Eligibility

Who can enroll

Minimum age40 Years
Maximum age70 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

Diagnosed with type 2 diabetes
BMI 28-35
Moderately preserved insulin secretory capacity (determined by glucagon test)

Exclusion criteria

Insulin treatment
Hypertension grade 3
Heart disease
Medical history with pancreatitis
Diagnosed with neuropathy
Excessive alcohol consumption
Any condition that would interfere with the protocol.

Endpoints (9)

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

Glycemic / diabetes
6
Weight & body composition
1
Other clinical outcomes
1
Other (unclassified)
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Body composition

Time frame:Before and after (3 days) Exercise intervention (12 weeks). Before and after 3 months of therapeutic semaglutide treatment

change from baseline, improvement

Glycemic / diabetes

6 endpoints
Primary/protocol endpoint/low confidence

Insulin secretion

Time frame:Change from baseline insulin secretion after Exercise intervention(12 weeks).

change from baseline, improvement

Primary/protocol endpoint

Insulin secretion

Time frame:Change from baseline insulin secretion after 3 months of therapeutic semaglutide treatment

change from baseline, improvement

Primary/protocol endpoint

Insulin secretion

Time frame:Change from baseline insulin secretion after 3 months of combined exercise and therapeutic semaglutide treatment

change from baseline, improvement

Secondary/protocol endpoint/low confidence

Insulin secretion

Time frame:Before and after (3 days) Exercise intervention (12 weeks). Before and after 3 months of therapeutic semaglutide treatment

descriptive, improvement

Secondary/protocol endpoint

insulin sensitivity

Time frame:Before and after (2 days) Exercise intervention(12 weeks). Before and after 3 months of therapeutic semaglutide treatment

HOMA-IR (insulin sensitivity)

change from baseline, improvement

Secondary/protocol endpoint

Glucose homeostasis

Time frame:Before and after (2 days) Exercise intervention (12 weeks). Before and after 3 months of therapeutic semaglutide treatment

HbA1c, change

change from baseline, improvement

LOINC 4548-4

Other clinical outcomes

1 endpoint
Secondary/protocol endpoint

Cardiorespiratory fitness

Time frame:Before and after (3 days) Exercise intervention (12 weeks). Before and after 3 months of therapeutic semaglutide treatment

change from baseline, improvement

Other (unclassified)

1 endpoint
Secondary/protocol endpoint/low confidence

Changes in plasma bone markers

Time frame:Before and after (2 days) Exercise intervention (12 weeks). Before and after 3 months of therapeutic semaglutide treatment

change from baseline, descriptive

Publications (1)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 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 1, 2026 snapshot.