Sit Less, Interact and Move More (SLIMM) 2 Study
Launched by SRINVASAN BEDDHU · Dec 20, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The Sit Less, Interact and Move More (SLIMM) 2 Study is a clinical trial aimed at helping people with chronic kidney disease and obesity reduce the time they spend sitting. Researchers have found that sitting for long periods can harm kidney function and increase the risk of diabetes and heart disease. This study, which is taking place at the University of Utah and Stanford University, is testing whether a combination of guided resistance training (to strengthen muscles) and a medication called semaglutide (which is often used for diabetes and weight loss) can help participants stick to a program that encourages them to move more and sit less.
To be eligible for this study, participants should have a specific level of kidney function, be able to perform resistance training, and have access to a smartphone or computer. The study is currently recruiting participants of all genders, aged 30 and older. Those who join can expect to receive guidance on exercising and using the medication while tracking their progress in reducing sedentary behavior. It's important to note that certain health conditions and recent medical treatments may disqualify individuals from participating, so a thorough screening will be conducted. Overall, the SLIMM 2 Study aims to find effective ways to promote movement and improve health in people with chronic kidney disease.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) Glomerular Filtration Rate (eGFR) 20 to \<60 mL/min/1.73m\^2
- • Able to perform resistance training
- • Access to compatible "smartphone" or device (i.e., Android, Kindle or Apple with internet connectivity or mobile network), desktop or laptop
- Exclusion Criteria:
- • Type 1 Diabetes
- • History of gastroparesis or paralytic ileus
- • At baseline, if sedentary time is 25 min/hr or less, measured by accelerometer
- • Potential contraindications to semaglutide such as a history of pancreatitis, and a family or personal history of multiple endocrine neoplasia type 2 or familial medullary thyroid carcinoma.
- • Previous bariatric surgery
- • Medical condition likely to limit survival to less than 1 year
- • Anticipated start of dialysis or kidney transplantation within 6 months
- • Any factors judged by the investigator or study team to likely limit adherence to interventions
- • Vulnerable populations- pregnant or incarcerated
- • Enrolled in interventional trials using drugs or devices
- • Not able to undergo informed consent
- • Recent hospitalizations or major interventional procedures done within the past 60 days
- • Known or suspected hypersensitivity to tegaderm
- • Use of any GLP-1 receptor agonist within 30 days prior to screening
- • Presently classified as being in New York Heart Association (NYHA) Class IV Heart Failure
- • Daytime use of supplemental oxygen (i.e., prescribed a stationary or portable oxygen system)
- • Presence of metastatic cancer
- • Current use of mobility aid(s)
- • Living in the same household of a participant already enrolled in the study
About Srinvasan Beddhu
Srinivasan Beddhu is a dedicated clinical trial sponsor committed to advancing medical research through innovative and rigorous study designs. With a focus on enhancing patient outcomes and safety, the organization specializes in conducting high-quality clinical trials across various therapeutic areas. Leveraging a team of experienced professionals and state-of-the-art methodologies, Srinivasan Beddhu aims to contribute to the development of effective treatments while adhering to the highest ethical standards and regulatory compliance. The sponsor's collaborative approach fosters partnerships with leading institutions and stakeholders, ensuring the successful execution of trials that address critical healthcare needs.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Stanford, California, United States
Salt Lake City, Utah, United States
Salt Lake City, Utah, United States
Patients applied
Trial Officials
Srinivasan Beddhu, M.D.
Principal Investigator
University of Utah
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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