MedTrace Logo

Feasibility of The Health Integrated Nutrition and Kidney Wellness Program

NCT07518719 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2026-04-09

No results posted yet for this study

Summary

Purpose of the Study:

This clinical trial will test whether a nutrition and kidney health program can work well for adults with kidney disease. The program was created with help from patients and community partners.

Main Questions:

How many eligible patients choose to join the program?

How many participants finish the full 12-week program?

How satisfied are participants with the program?

What Participants Will Do:

Participants will be assigned to a diet-focused lifestyle education series (THINK-Well Intervention) or enhance usual care.

THINK-Well Intervention group will take part in 7 group education sessions over 12 weeks. Sessions will be online and in-person. Topics include eating to promote heart-kidney-and metabolic health, managing long-term health conditions, setting health goals, and sharing experiences with others who have chronic disease. Participants will practice meal preparation through cooking classes and have opportunity to apply lessons on choosing whole foods with food bucks provided.

The enhanced usual care group will receive two virtual nutrition education sessions led by a trained educator over 12 weeks. Topics will be similar to standard education provided to people with kidney disease managed by a kidney doctor. Topics will be adapted from established resources from the National Kidney Foundation, American Kidney Fund, and American Heart Association.

Conditions

Interventions

BEHAVIORAL

THINK-Well

Seven hybrid (online or in-person) group nutrition education sessions paired with food bucks and one individual consultation with a dietitian over 12-weeks.

OTHER

Enhanced Usual Care

Two virtual group nutrition educational sessions provided by a trained educator.

Sponsors & Collaborators

Principal Investigators

  • Linda-Marie U Lavenburg, DO, MS · University of Pittsburgh

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-29
Primary Completion
2026-10-31
Completion
2026-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07518719 on ClinicalTrials.gov