Obesity & OverweightPhase 3EXER-MEDNCT07298915
The Effect of Exercise and Tirzepatide on Weight and Health Outcomes (EXER-MED)
A Phase 3 study testing Tirzepatide and Exercise in people with Obesity & Overweight, run by University of Virginia at 1 site in United States.
Trial summary
This is clinical trials is to evaluate the effect of exercise with weight loss medication compared to weight loss alone. The study will enroll 24 adults from 30-65 years old with overweight or obesity. Read more about this study
- Who is it for?
- Ages 30 to 65 years
- Conditions the study is for
- Obesity & Overweight
- What is being tested?
- Tirzepatide and Exercise
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 24 participants
- Where
- 1 siteUnited States
- Study dates
- Aug 2026to Jun 2027
- Phase
- Phase 3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Men and women 30-65 years of age, postmenopausal women included
- 27-29.9 with an additional CVD risk factor or 30-40 kg/m2
- For overweight adults only: additional cardiometabolic risk factor (diagnosed dyslipidemia, hypertension)
- Willingness and adequate health to go on weight loss medication
- The capability and willingness to provide written informed consent
- Approval of their primary care provider to go on weight loss medication
Who cannot join
- Including but not limited to serious arrhythmias
- Cardiomyopathy
- Congestive heart failure
- Stroke or transient ischemic attacks
- Peripheral vascular disease
- Previous history of myocardial infarction or stroke
Show all 18Show fewer
- Previous diagnosis or taking medication for type 1 or 2 diabetes, fasting glucose >125 mg/dL or HbA1C ≥6.5%
- Systolic blood pressure >160 mmHg and diastolic blood pressure >100 mmHg.
- Hospitalization for mental illness within the past 5 years or currently undergoing treatment for severe mental illness
- Conditions that can be aggravated or are contraindicated by exercise training
- Plans to be out of town more than 3 weeks in the next 4 months.
- Currently pregnant or plans to become pregnant
- Currently in a diet or exercise program
- Non-compliance during screening or extreme difficulty in obtaining baseline blood samples
- Enrolled in a different exercise program
- Previous weight loss surgery
- Use of weight loss medication within the last year
- hypo/hyper thyroid (medicated or unmedicated)
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
University of Virginia
Charlottesville, Virginia, 22901
Damon L Swift, Ph.D., (434) 924-1436
Damon L Swift, Ph.D.
About this study
This is clinical trials is to evaluate the effect of exercise with weight loss medication compared to weight loss alone. The study will enroll 24 adults from 30-65 years old with overweight or obesity.
The main questions it will answer includes:
Read more
- Does exercise combined with weight loss medication reduce body weight and body fat more than weight loss medication alone
- Does exercise combined with weight loss medication improve other risk factors more such as the sugar in the blood, cholesterol, fitness, and quality of life
Participants will:
- Take a weight loss medication (tirzepatide) monthly under the supervision of their primary care physician
- (Exercise group only) Will perform exercise ~3 times a week at the University of Virginia). Walking on a treadmill and resistance training
- Visit the study site at the beginning of the study and after the study to evaluate weight, body fat, and other health measures
Read the detailed description
The new type class of weight loss medications called GLP-1 medications have been shown to cause weight loss and improve risk factors for heart disease and diabetes. One thing that is currently unknown is whether exercise augments the impact of weight loss in people taking GLP-1 medication. The EXER-MED study is a pilot study evaluating the effect of 16 weeks of exercise training with GLP-1 medication compared to taking the medication alone. We will evaluate the impact of the study groups on weight, body composition (percent fat, percent lean mass), blood pressure, arterial stiffness, blood work (cholesterol, blood pressure, glucose, insulin) and quality of life.
- Conditions
- Obesity & Overweight
- Being tested
- Tirzepatide, Exercise
- Keywords
- Obesity, Overweight, Exercise, aerobic, resistance training, GLP-1, Weight loss
- Medical subject headings
- Obesity, Overweight, Motor Activity, Weight Loss
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TirzepatideDrug
Participants will take tirzepatide under the care of their primary care provider for 16 weeks
ExerciseBehavioural
Participants will perform a combination of aerobic and resistance training for 16 weeks
| Study group | Role | What they receive |
|---|---|---|
| Exercise | Experimental | Participants will perform aerobic and resistance exercise while taking monthly tirzepatide for 16 weeks Receives: Drug: Tirzepatide; Behavioral: Exercise |
| Standard Care | Active comparator | Participants will take monthly Tirzepatide under the care of their primary care provider for 16 weeks Receives: Drug: Tirzepatide |
What is being measured
The primary outcome is the main question the study is designed to answer.
Weight
Measurement will be taken 3 times and measured in kg. A positive value indicates an increase in weight and a negative value indicates a reduction in weight
Measured: Baseline and 16 Weeks
Secondary outcomes (14)
Physical activity level
Physical activity will measured via accelerometry (total steps and light, moderate, vigorous physical activity) and steps for 7 consecutive days
Measured: Baseline and 16 weeks
Changes in Blood Lipids Concentrations
A fasting blood sample will be used to measure low density lipoprotein, high density lipoprotein, total cholesterol, and triglycerides will be measured. It will be quantified as the specific amount of the lipoprotein within the blood in mg/dL for all lipid variables. Participants will be fasted at least 12 hours prior to the blood draw. Change will be quantified as the week 16 value subtracted from the baseline value. A positive value indicates an increase in the blood lipid variable and a negative value is associated with a reduction in the variable.
Measured: Baseline to 16 weeks
Resting Metabolic Rate
Resting metabolic rate (RMR) will be measured in a quiet, temperature-controlled room using indirect calorimetry with a clear ventilated canopy and dilution pump. An increase represents a positive change and a decrease represents a negative change
Measured: Baseline and 16 Weeks
Change in Fasting Glucose Level
Change in fasting glucose level. Fasting glucose level refers to the concentration of glucose within the blood (mg/dL). The change in fasting glucose level is quantified by subtracting the week 16 value from the baseline value. Thus, a positive value indicates an increase in glucose level and a negative value indicates a decrease in glucose.
Measured: Baseline to 16 Weeks
Change in Fasting Insulin Level
Fasting insulin represents the concentration of insulin in the blood. A positive value represents an increase in insulin concentration and a negative value represents a decrease in insulin concentration.
Measured: Baseline to 16 Weeks
Change in Augmentation Index
Central Arterial stiffness will be measured using a SphygmoCor XCEL (Itasca, IL). Participants will refrain from large meals and caffeine for at least 2 hours and alcohol, vigorous exercise and vasoactive medication for at least 12 hours. Testing will occur in a quiet temperature controlled room in the seated position after a 5 minute rest. Augmentation index represent central arterial stiffness and will be quantified via augmentation index (%). The augmentation index (AIx) is a measure of systemic arterial stiffness, and is defined as the ratio of augmentation (Δ P) to central pulse pressure and expressed as percent. AIx = (ΔP/PP) x 100, where P = pressure and PP = Pulse Pressure. A lower value indicates better stiffness
Measured: Baseline to 16 Weeks
Changes in Blood Pressure (mmHg)
Brachial and aortic blood pressure will be measured using a sphygmocor XCEL. Blood pressure is quantified in mmHg and will be taken in the seated position after a 5 minute rest. Change in blood pressure is quantified by subtracting the week 10 value from the baseline value. Thus, a positive number is associated with an increase in blood pressure across the time point and a decrease indicates a decrease in blood pressure
Measured: Baseline to 16 weeks
Change in hemoglobin A1C
Hemoglobin A1C (%) will be measured at baseline and 16 weeks. Change in hemoglobin A1C will be determined by subtracting the week 16 value from baseline. A positive change indicates and increase in hemoglobin A1C and a negative value indicates a decrease in hemoglobin A1C.
Measured: Baseline and Week 16
Change in Waist Circumference
Waist circumference will be measured at the natural waist (midway between the inferior border of the rib cage and the superior aspect of the iliac crest) with a gulick tape measure. Both landmarks (the inferior border of the ribcage and the superior aspect of the iliac crest) will be marked and the distance will be measured to determine the appropriate measurement site. Staff will confirm that: 1) the measurement tape remains horizontal; 2) the tape touches the entire circumference of the participant; 3) abdominal tissue is not compressed; 3) the tape measure is not within abdominal folds; 4) the measurement is taken at the end of normal respiration. The measurement will be repeated an additional time, and the reported value will be the average of these measurements. Both measurements must be within 0.5 cm to be considered acceptable for data purposes. The change in waist circumference will be quantified as the the week 16 value subtracted from the baseline value
Measured: Baseline to Week 16
Change in Body Composition (Fat mass or Lean Mass)
Dual-energy X-ray absorptiometry will be used to measure changes in fat mass and lean mass. Body fat will be quantified as the percent of fat relative to the total body composition. Lean mass will be quantified as the percent of lean tissue relative to the total body composition. Change in these variables will be quantified as by subtracting the week 16 value from the baseline value. Thus, a change in positive direction is associated with an increase in body fat or lean mass and a negative value represent a decrease.
Measured: Baseline to Week 16
Change in Cardiorespiratory Fitness
Fitness will be measured using a modified Balke protocol on a treadmill. Participants will walk at an initial speed of 2.0 mph with 0% grade for the first 3 minutes after which the treadmill speed will increase to 3.0 mph for the next 3 minutes. The treadmill grade will be increased by 2.5% every 3 minutes until volitional exhaustion. Fitness will be quantified in absolute terms (VO2) L/min, relative (VO2 mL/kg/min) and Estimated METs. Change in fitness will be quantified by subtracting the week 16 value from the baseline value. A positive value will indicate and increase in fitness. A negative value will indicate a reduction in fitness.
Measured: Baseline and 16 Weeks
Change in dietary quality
Dietary quality is measured with the ASA 24-hour dietary recall (ASA 24) . The ASA 24 is web-based tool that allows individuals to self-report all foods and beverages consumed in the previous 24 hours (i.e., the data collection method). This allows us to track diet quality changes over time. Change in dietary outcomes will be quantified by subtracting week 16 values from baseline. A positive value will represent an increase in a variable. A negative value will represent a reduction in a variable.
Measured: Baseline to Week 16
Quality of Life (IWQL-Lite)
Measured by the questionnaire Impact of Weight on Quality of Life-Lite (IWQL-Lite) at baseline and Week 16. Scores range from 0 to 100, with 100 representing the best quality of life. Change in quality of life will be expressed by subtracting Week 16 from baseline level. An increase in quality of life will be represented by a positive value. A negative value represents a reduction in quality of life.
Measured: Baseline to Week 16
Change in isokinetic dynamometry
Isokinetic knee flexor and extensor muscles strength and endurance will be evaluated with the isokinetic dynamometer. Change in strength and endurance outcomes will be quantified by subtracting the the Week 16 value from the baseline value. A positive value will indicate an increase in strength or endurance. A negative value will indicate a reduction in strength or endurance.
Measured: Baseline and Week 16
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Dec 2025
- Study startAug 2026 (estimated)
- Primary completionDec 2026 (estimated)
- Study completionJun 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obesity & OverweightStudies of the same condition, open and under way.
- More trials run by University of VirginiaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 24 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Virginia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Damon Swift, University of Virginia
- Investigators
- Damon L Swift, Ph.D, Principal investigator, University of Virginia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07298915
- Sponsor's protocol ID
- 302929
- Acronym
- EXER-MED
- Status last verified
- May 2026
- First submitted
- 19 Dec 2025
- Last updated
- 6 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Exercise and Tirzepatide on Weight and Health Outcomes (EXER-MED)
- ClinicalTrials.gov ID
- NCT07298915
- Acronym / sponsor ID
- EXER-MED / 302929
- Conditions
- Obesity & Overweight
- Keywords
- Obesity, Overweight, Exercise, aerobic, resistance training, GLP-1, Weight loss
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 24 participants (estimated)
- Lead sponsor
- University of VirginiaUniversity, hospital or other
- Study start
- Aug 2026 (estimated)
- Primary completion
- Dec 2026 (estimated)
- Study completion
- Jun 2027 (estimated)
- First posted
- 23 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is clinical trials is to evaluate the effect of exercise with weight loss medication compared to weight loss alone. The study will enroll 24 adults from 30-65 years old with overweight or obesity.
The main questions it will answer includes:
- Does exercise combined with weight loss medication reduce body weight and body fat more than weight loss medication alone
- Does exercise combined with weight loss medication improve other risk factors more such as the sugar in the blood, cholesterol, fitness, and quality of life
Participants will:
- Take a weight loss medication (tirzepatide) monthly under the supervision of their primary care physician
- (Exercise group only) Will perform exercise ~3 times a week at the University of Virginia). Walking on a treadmill and resistance training
- Visit the study site at the beginning of the study and after the study to evaluate weight, body fat, and other health measures
Detailed description
The new type class of weight loss medications called GLP-1 medications have been shown to cause weight loss and improve risk factors for heart disease and diabetes. One thing that is currently unknown is whether exercise augments the impact of weight loss in people taking GLP-1 medication. The EXER-MED study is a pilot study evaluating the effect of 16 weeks of exercise training with GLP-1 medication compared to taking the medication alone. We will evaluate the impact of the study groups on weight, body composition (percent fat, percent lean mass), blood pressure, arterial stiffness, blood work (cholesterol, blood pressure, glucose, insulin) and quality of life.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Exercise | Experimental | Drug: Tirzepatide, Behavioral: ExerciseParticipants will perform aerobic and resistance exercise while taking monthly tirzepatide for 16 weeks |
| Standard Care | Active comparator | Drug: TirzepatideParticipants will take monthly Tirzepatide under the care of their primary care provider for 16 weeks |
Who may qualify
- Ages
- 30 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Men and women 30-65 years of age, postmenopausal women included
- 27-29.9 with an additional CVD risk factor or 30-40 kg/m2
- For overweight adults only: additional cardiometabolic risk factor (diagnosed dyslipidemia, hypertension)
- Willingness and adequate health to go on weight loss medication
- The capability and willingness to provide written informed consent
Key exclusion criteria (18 listed)
- Including but not limited to serious arrhythmias
- Cardiomyopathy
- Congestive heart failure
- Stroke or transient ischemic attacks
- Peripheral vascular disease
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| TirzepatideParticipants will take tirzepatide under the care of their primary care provider for 16 weeks | Drug | Exercise, Standard Care |
| ExerciseParticipants will perform a combination of aerobic and resistance training for 16 weeks | Behavioural | Exercise |
Primary outcome
Weight
Time frame: Baseline and 16 Weeks
Measurement will be taken 3 times and measured in kg. A positive value indicates an increase in weight and a negative value indicates a reduction in weight
14 secondary outcomes
Physical activity level
Time frame: Baseline and 16 weeks
Changes in Blood Lipids Concentrations
Time frame: Baseline to 16 weeks
Resting Metabolic Rate
Time frame: Baseline and 16 Weeks
Change in Fasting Glucose Level
Time frame: Baseline to 16 Weeks
Change in Fasting Insulin Level
Time frame: Baseline to 16 Weeks
Change in Augmentation Index
Time frame: Baseline to 16 Weeks
Changes in Blood Pressure (mmHg)
Time frame: Baseline to 16 weeks
Change in hemoglobin A1C
Time frame: Baseline and Week 16
Change in Waist Circumference
Time frame: Baseline to Week 16
Change in Body Composition (Fat mass or Lean Mass)
Time frame: Baseline to Week 16
Change in Cardiorespiratory Fitness
Time frame: Baseline and 16 Weeks
Change in dietary quality
Time frame: Baseline to Week 16
Quality of Life (IWQL-Lite)
Time frame: Baseline to Week 16
Change in isokinetic dynamometry
Time frame: Baseline and Week 16
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 May 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Damon L Swift, Ph.D principal investigator
University of Virginia
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Tirzepatide and Exercise in people with Obesity & Overweight, run by University of Virginia at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 18 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 6 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Damon L Swift, Ph.D. ((434) 924-1436, dls3s@virginia.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Weight (time frame: Baseline and 16 Weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2026.