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Search / Trial NCT06861439

GLP-1s to Enhance Lasting Optimal Weight

Launched by WAKE FOREST UNIVERSITY HEALTH SCIENCES · Feb 28, 2025

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Weight Loss Muscle Loss Physical Disability Bone Density Older Adults

ClinConnect Summary

This clinical trial, called "GLP-1s to Enhance Lasting Optimal Weight," is looking at how a medication called tirzepatide can help older adults with obesity. The study will last for nine months and aims to understand how this medication affects body composition, bone health, and physical performance. Participants will take tirzepatide once a week and attend regular check-ins with their study doctor and a dietitian, either in person or via video calls. They will also join group sessions twice a month, track their daily steps with an activity tracker, and weigh themselves daily using a smart scale. Additionally, participants will keep a record of their food and drink intake.

To be eligible for the study, participants should be between 23 and 74 years old, have a body mass index (BMI) between 27 and 37, and live independently. They need to be able to get to study visits and agree to follow the study's procedures. However, some individuals may not qualify, including those who have certain medical conditions, use certain medications, or have significant mobility issues. This trial is not yet recruiting participants, but it offers a structured way for eligible individuals to potentially improve their weight and overall health with the support of healthcare professionals.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • BMI 30-37 kg/m2 or BMI 27-\<30 kg/m2 with at least 1 weight-related comorbidity
  • community dwelling
  • able to provide own transportation to study visits
  • willing to provide informed consent
  • willing to take terzepatide for 9 months
  • agree to all study procedures/assessments
  • approved for participation by the study physician
  • Exclusion Criteria:
  • dependent on a cane or walker or needing assistance with any activity of daily living
  • history of mild cognitive impairment or dementia or cognitive impairment on Montreal Cognitive Assessment (MoCA score \<22)
  • evidence of depressive symptoms (Center for Epidemiologic Studies Depression scale score =\>16
  • use of \>1 tobacco product/day or 4/week or vaped \>1/week in past year
  • excessive alcohol use in past month (\>7 drinks/week for women; \>14 drinks/week for men)
  • weight loss or gain \>5% in past 3 months
  • vegan or other severe dietary restriction
  • history of binge eating disorder
  • regular participation in high intensity aerobic or resistance exercise training \>150 mins/week
  • severe arthritis, fracture, chronic injury, or other musculoskeletal disorder that prevents walking independently
  • joint replacement or other orthopedic surgery in past 6 months or planned in next 12 months
  • osteoporosis (self report or DXA t-score \<= -2.5 on total hip and/or femoral neck)
  • uncontrolled hypertension (systolic \>160 OR diastolic \>100 mmHg) upon repeated assessments
  • type 1 diabetes
  • uncontrolled type 2 diabetes (HbA1c \>7.5%), type 2 diabetes diagnosed within last year, or newly identified type 2 diabetes (HbA1c \>6.5%)
  • dialysis or abnormal kidney function (eGFR \<30 ml/min/1.73m2)
  • liver disease or abnormal liver function (ALT levels 2 times above normal limit)
  • severe anemia (Hb \<11 g/dL)
  • potassium or sodium above or below normal limits
  • uncontrolled thyroid disease (hypo/hyper) or requiring recent (past 3 months) adjustments in thyroid hormone supplementation or TSH \<0.45 or \>4.5 mU/L
  • stroke, heart attack, heart failure hospitalization, or revascularization procedure within the past year; New York heart failure Class \>2; COPD requiring oxygen use; uncontrolled angina; PAD diagnosis within the last year; progressive neurologic disease (e.g., Parkinson's, ALS, MS); other diseases suggesting a life-expectancy \<3 years
  • personal or family history of medullary thyroid carcinoma, history of multiple endocrine neoplasia syndrome type 2, or any other cancer (except non-melanoma skin cancers) requiring treatment in past year
  • history of gastroparesis or pancreatitis
  • cholelithiasis, severe irritable bowel syndrome or Crohn's disease
  • history of stomach or small intestinal surgery (except appendectomy but including surgery for weight loss)
  • recent (within 4 weeks) acute respiratory illness including influenza, COVID-19
  • overnight hospitalization within the past 6 months
  • regular use of growth hormones, medications prescribed for weight management, prescription osteoporosis medications, certain prescription medications for diabetes including insulin, sulfonylurea, meglitinides, GLP-1 agonists, SGLT2 inhibitors
  • use of oral steroids for \>1 month within the last 3 months
  • current participation in another intervention research study
  • planned out of town trips greater than 3 weeks in the next year

About Wake Forest University Health Sciences

Wake Forest University Health Sciences is a leading academic research institution dedicated to advancing healthcare through innovative clinical trials and translational research. With a strong emphasis on multidisciplinary collaboration, the organization leverages its extensive expertise in medical research, patient care, and education to develop and evaluate new therapies and interventions. Committed to improving patient outcomes and public health, Wake Forest University Health Sciences fosters a dynamic environment for scientific inquiry, engaging in a wide range of clinical studies that address pressing health challenges. Through its rigorous methodologies and ethical standards, the institution aims to contribute significantly to the medical field and enhance the quality of life for diverse populations.

Locations

Winston Salem, North Carolina, United States

Patients applied

0 patients applied

Trial Officials

Denise Houston, PhD

Principal Investigator

Atrium Health Wake Forest Baptist

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported