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Musculoskeletal AbnormalitiesPhase 4GRAMSNCT07154719

GLP-1R Actions on Muscle and the Skeleton

A Phase 4 study testing Tirzepatide and Lifestyle toolkit in people with Musculoskeletal Abnormalities and Obesity, run by Pennington Biomedical Research Center at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The GRAMS study objectives are to assess the musculoskeletal changes that occur after weight loss using GLP-1 based therapy. A lifestyle intervention with diet and exercise is included to assess any mitigating effects are provided, versus a control group with regular exercise and diet. Read more about this study

Who is it for?
Ages 18 to 50 years
What is being tested?
Tirzepatide and Lifestyle toolkit
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
50 participants
Where
2 sitesUnited States
Study dates
9 Oct 2025to 1 May 2027
Phase
Phase 4
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 18 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Subjects will have a BMI between 30kg/m2
  • 40kg/m2 (inclusive)
  • Be between 18 and 50 years of age (inclusive).
  • Non-Hispanic Black males and females will be enrolled at PBRC.
  • Rural males and females will be enrolled at MaineHealth.
  • Female subjects will be premenopausal.
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  • Females have had their last menstrual period less than 60 days before screening.
  • Females have the absence of menopausal-associated vasomotor symptoms.
  • All subjects must be able to use Lifestyle Toolkit as prescribed for intervention arm.

Who cannot join

  • Males and females over the age of 50 years of age
  • Menopausal females.
  • Subjects on systemic corticosteroids or other agents known to increase loss of muscle and bone mass.
  • Subjects who are on medications that increase or decrease weight status.
  • Subjects having contraindications to tirzepatide in the package insert.
  • Subjects with a history of malignancy other than non-melanoma skin cancer
Show all 22Show fewer
  • Subjects with known osteoporosis or are on osteoporosis therapies (gonadal hormones or hormone antagonists).
  • Subjects with uncontrolled thyroid or parathyroid disease that may influence the study results.
  • Subjects with a clinically significant hematologic abnormality, kidney disease, liver disease, or diabetes.
  • Females of childbearing potential who do not agree to using an effective method of contraception during the study. Medically acceptable methods include oral contraceptive medication, an intrauterine device (IUD), an implantable contraceptive (such as Implanon), or a barrier method (such as condom or diaphragm with spermicide).
  • Injectable contraceptives such as Depo-Provera are a cause for exclusion in that they can cause bone loss.
  • Abstinence is acceptable, as is sexual activity exclusively with same sex partners.
  • Fertility Appreciation Based Methods (natural family planning) are also acceptable forms of addressing childbearing potential in all subjects. A urine pregnancy test (UPT) will be performed on all females of childbearing potential at the screening visit, 3 and 6 months.
  • Unable to follow Lifestyle Toolkit as prescribed for intervention arm.
  • Patient Health Questionnaire-9 (PHQ-9) Score equal to or greater than 15 (clinical depression).
  • Adults who are unable to consent.
  • Individuals who are not yet adults (infants, children and teenagers).
  • Pregnant females.
  • Incarcerated individuals.
  • Contraindication to MRI - including but not limited to non-removable metallic or electronic implants, claustrophobia or other fear of confinement, inability to tolerate loud scanner noise, body weight greater than 500 pounds.
  • Subjects with a baseline level of 25-OH vitamin D <15 ng/ml will be excluded from the trial. The subject's physician will be notified, and the subject will be referred to their primary care physician.
  • Any significant EKG abnormalities that are considered a risk for utilizing weight management therapies.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Adithya Hari, MD contact

225-763-2966

Adithya.Hari@pbrc.edu

Yanna X Alesafis de Koter, MPH contact

yanna.dekoter@pbrc.edu

United States2 sites, 1 recruiting
  • Pennington Biomedical Research Center

    Baton Rouge, Louisiana, 70808

    Active, not recruiting
  • MaineHealth Center for Clinical and Translational Science

    Scarborough, Maine, 04074

    Irwin Brodsky, MD, MPH, 207-396-7700, irwin.brodsky@mainehealth.org

    Sarah Eastman, 207-396-8138, sarah.eastman@mainehealth.org

    Recruiting

Other trials in United States

About this study

The GRAMS study objectives are to assess the musculoskeletal changes that occur after weight loss using GLP-1 based therapy. A lifestyle intervention with diet and exercise is included to assess any mitigating effects are provided, versus a control group with regular exercise and diet.

Read the detailed description

Obesity and type 2 diabetes remain at epidemic proportions in our country particularly in vulnerable populations such as elderly, and minority patients. Over the last 20 years, the use of incretin-based agents (Glucagon-like Peptide 1 Receptor Agonist (GLP-1 RA) and Glucose dependent insulinotrophic polypeptide (GIP) to treat these disorders has offered unprecedented advances based on significant weight loss and reduction in major cardiovascular endpoints. Whilst weight loss provides a vital aspect for addressing obesity and type 2 diabetes, there are concerns associated with the quality of weight reduction.

The impact of losing weight on the musculoskeletal system has garnered recent attention in the lay press. Reported high-impact studies have reported excessive loss of skeletal muscle using GLP-1 RAs. The data regarding combined therapies (GLP-1 RA and GIP) suggested smaller loses. This preliminary data is based on using a surrogate marker (fat-free mass) determined by dual energy x-ray absorptiometry (DXA).

Recent reviews evaluating the impact that incretin-based agents have on fat-free-mass were found to be inconclusive based on high variability and multiple confounding factors. Assessing the impact that these agents have on the musculoskeletal system is now an important endeavor. (Aim 1-2) Diet-induced weight loss is also associated with bone loss, although little attention has focused on this potentially problematic outcome. In the CALERIE study, modest caloric restriction (15%) over two years led to weight loss and a 2% reduction in hip bone mineral density (BMD) among normal weight individuals. The mechanisms of weight loss-induced bone loss are unclear, although a drop in fat-free mass (which is composed of skeletal muscle, organs, water and connective tissues) principally muscle, such as occurs with the GLP1RAs, may predispose to injury, disability and bone loss. Another possibility is a mechanical form of skeletal adaptation to lower lean mass, through myokine mediated bone remodeling. However, significant trabecular bone loss in a non-weight bearing skeletal site occurs in mice as the investigators have shown in the mandible, from a 30% CR diet (Liu, personal communication). As such gravitational unloading due to weight loss is not solely responsible for deleterious skeletal changes. Despite the dramatic weight and lean mass loss from the GLP1 RAs, few clinical trials have focused on loss of muscle mass and fewer on any skeletal changes. In those that did, the results suggest equipoise for skeletal changes. There are no data on the skeletal effects from tirzepatide which can drive up to 25% weight loss. (Aim 1c) Also, it is unknown whether the addition of dietary modifications and resistance-based exercises impacts skeletal adaptation, muscle mass and bone loss. (Aim 2) Furthermore, there are inconsistent data in non-Hispanic Blacks with the GLP1 RAs because trial participation in under-represented populations has been poor. Hence, there is a major knowledge gap in our understanding the impact that a mixed GIP and GLP1RA, tirzepatide affects muscle and bone mass, particularly among underserved populations.

The wide-spread usage of GLP-1 related agents has not required formal recommendations regarding the use of exercises, specifically resistance-based exercises, or dietary protein optimization to address the potential for loss of fat-free mass or bone mineral density that has been suggested in studies evaluating body composition and bone density in subjects using these compounds. While the data for using such lifestyle interventions with diet and bariatric surgery have confirmed benefits in reducing loss of fat-free mass, the investigators know of only 1 published report using GLP-1 agents and exercise: Lundgren et al. found that in subjects using additional resistance-based exercise had a more favorable impact on sparing fat-free mass.

Additional gaps in our understanding remain despite the growing use and popularity of these agents. Additionally, patients with obesity and type 2 diabetes tend to develop ectopic fat within muscle (myosteatosis) that is not measured as part of fat free mass by DXA. It is posited that the major depot for acute loss of skeletal muscle from rapid weight loss may be from this portion of poor-quality lipid-rich tissue quelling major concerns. (Aim 2b) Aim 3, an explorative outcome, the investigators will determine if tirzepatide causes bone loss by measuring bone formation (P1NP) and bone resorption markers (NTx), if imbalanced skeletal remodeling is related to the change in total lean mass, muscle mass through reduced myokine (i.e., irisin) release, skeletal adaptation to weight change or another endocrine mechanism. Using a team science approach, the investigators will combine the expertise in metabolism and body composition of the PBRC group with skeletal expertise from MaineHealth to provide key insights into musculoskeletal effects from tirzepatide, a relatively new but often sought after drug for weight loss and type 2 diabetes. This supplement could also shed light on newer mechanisms of weight loss-induced bone loss and set the stage for a larger clinical trial.

Being tested
Tirzepatide, Lifestyle toolkit
Keywords
GLP-1 agonists, Obesity treatments, Muscleskeletal loss, Tirzepatide
Medical subject headings
Musculoskeletal Abnormalities, Obesity, Osteoporosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TirzepatideDrug

    GLP-1 based treatment for obesity

  • Lifestyle toolkitBehavioural

    2 ABBOTT protein shakes daily and resistance-based exercise x 3 days per week.

Study groups in NCT07154719
Study groupRoleWhat they receive
Treatment/intervention groupExperimentalTreatment with Tirzepatide for 5 months and lifestyle toolkit.
Receives: Drug: Tirzepatide
Control/PlaceboPlacebo comparatorTreatment with Tirzepatide for 5 months with regular diet and exercise.
Receives: Behavioral: Lifestyle toolkit

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in fat free mass (FFM) using DXA imaging. FFM equals all body composition that is not fat mass. This includes bone, skeletal muscle, organs, water and all connective tissues. The unit of measurement is in kilograms (kg) at baseline, 3 and 6 mo.

    DXA (Dual energy Xray absorptiometry)

    Measured: Baseline and time 3, and 6 months.

Secondary outcomes (6)
  1. MRI (thigh) without contrast

    To assess for muscle quality (% of skeletal muscle to intermuscular fat)

    Measured: Month 1 (baseline), month 3, month 6 (final visit)

  2. Osteocalcin

    Blood draw, metabolism biomarker

    Measured: Month 1 (baseline), month 3, month 6 (final visit)

  3. Irisin

    Blood draw, bone health biomarker

    Measured: Month 1 (baseline), month 3, month 6 (final visit)

  4. Procollagen 1 N-terminal peptide (P1NP)

    Blood draw, bone health biomarker

    Measured: Month 1 (baseline), month 3, and month 6 (final visit)

  5. C-Terminal Telopeptide of type I collagen (CTX-1)

    Blood draw, bone health biomarker

    Measured: Month 1 (baseline), month 3, month 6 (final visit)

  6. Insulin-like Growth Factor 1 (IGF-1)

    Blood draw, bone health biomarker

    Measured: Month 1 (baseline), month 3, month 6 (final visit)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Sep 2025
  2. Study start9 Oct 2025
  3. Primary completion1 Feb 2027 (estimated)
  4. Study completion1 May 2027 (estimated)

Resources

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 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
The investigators will enroll 25 subjects in each study arm. Both arms will involve treatment with a GLP-1 agonist (tirzepatide) for 5 months. The intervention arm will use a lifestyle toolkit which includes protein supplements and resistance-based exercises. The control group will use regular diet and exercise activities. Testing includes DXA and MRI body composition as well as lab tests to assess for muscle skeletal quality and physical fitness.
Masking
None (open label)
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07154719
Sponsor's protocol ID
PBRC 2024-031
Acronym
GRAMS
Status last verified
Aug 2026
First submitted
22 Aug 2025
Last updated
27 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Sharing plan of data will be completed by primary study team by 12/01/25. All details will be provided by PI and study team.

Publications

  • Goodpaster BH, Theriault R, Watkins SC, Kelley DE. Intramuscular lipid content is increased in obesity and decreased by weight loss. Metabolism. 2000 Apr;49(4):467-72. doi: 10.1016/s0026-0495(00)80010-4.

    PubMed 10778870
  • Lundgren JR, Janus C, Jensen SBK, Juhl CR, Olsen LM, Christensen RM, Svane MS, Bandholm T, Bojsen-Moller KN, Blond MB, Jensen JB, Stallknecht BM, Holst JJ, Madsbad S, Torekov SS. Healthy Weight Loss Maintenance with Exercise, Liraglutide, or Both Combined. N Engl J Med. 2021 May 6;384(18):1719-1730. doi: 10.1056/NEJMoa2028198.

    PubMed 33951361
  • Jastreboff AM, Aronne LJ, Ahmad NN, Wharton S, Connery L, Alves B, Kiyosue A, Zhang S, Liu B, Bunck MC, Stefanski A; SURMOUNT-1 Investigators. Tirzepatide Once Weekly for the Treatment of Obesity. N Engl J Med. 2022 Jul 21;387(3):205-216. doi: 10.1056/NEJMoa2206038. Epub 2022 Jun 4.

    PubMed 35658024
  • Dubin RL, Heymsfield SB, Ravussin E, Greenway FL. Glucagon-like peptide-1 receptor agonist-based agents and weight loss composition: Filling the gaps. Diabetes Obes Metab. 2024 Dec;26(12):5503-5518. doi: 10.1111/dom.15913. Epub 2024 Sep 30.

    PubMed 39344838

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Tirzepatide and Lifestyle toolkit in people with Musculoskeletal Abnormalities and Obesity, run by Pennington Biomedical Research Center at 2 sites 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 9 inclusion and 22 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: looking for participants now, as of the sponsor's last update on 27 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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. Some participants in this study may receive a placebo. 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

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 Adithya Hari, MD (225-763-2966, Adithya.Hari@pbrc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in fat free mass (FFM) using DXA imaging. FFM equals all body composition that is not fat mass. This includes bone, skeletal muscle, organs, water and all connective tissues. The unit of measurement is in kilograms (kg) at baseline, 3 and 6 mo. (time frame: Baseline and time 3, and 6 months.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07154719, which also lists 4 linked publications.

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 27 Aug 2026.

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