Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06924177

UTSW NORC Pilot Spinal Cord Injury Dietary Program

Led by University of Texas Southwestern Medical Center · Updated on 2026-03-31

20

Participants Needed

1

Research Sites

15 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to learn about the effects of a 9-week dietician-guided program modified from the National Diabetic Prevention Program (modified DPP-diet) in people with spinal cord injury on body composition and insulin sensitivity. The main question it aims to answer is: Does 9 week modified DPP-diet reduce body fat percentage and insulin resistance? Participants will: Have 9 weeks of Telehealth visit with dietician certified in providing DPP. Visit the laboratory before, immediately and 9 weeks after completion of the modified DPP-diet. Share with the researcher on the perceived benefit and obstacles in implementing the modified DPP-diet as part of their daily activities.

CONDITIONS

Official Title

UTSW NORC Pilot Spinal Cord Injury Dietary Program

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 65 years old
  • Have had spinal cord injury for more than one year
  • Not independently ambulatory
  • Primarily use a wheelchair for mobility
  • Live in the community
  • Do not have any exclusionary medical conditions
Not Eligible

You will not qualify if you...

  • Uncontrolled type 2 diabetes mellitus
  • Pregnancy
  • Active systemic diseases such as heart disease, kidney failure or insufficiency, multiple myeloma, lupus with nephropathy, sickle cell disease, symptomatic myasthenia gravis, or poorly controlled thyroid disorders

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Texas Southwestern Medical Center

Dallas, Texas, United States, 75390-8878

Actively Recruiting

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Research Team

Y

Yi-Ting Tzen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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