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NCT05468437Active, not recruiting

Telenutrition for Individuals With SCI

Telenutrition to Improve Cardiometabolic Health and Quality of Life Among Individuals With Spinal Cord Injury

Source: ClinicalTrials.gov · Last updated 1 Sept 2026

Brief summary (registry, in English)

This study will provide nutrition counseling via FaceTime on an iPad to persons with traumatic spinal cord injury (SCI) who are overweight or obese and are at least one-year post-injury. Nutrition counseling may help participants to develop eating behaviors that match the participants' needs and help improve heart health. The purpose of this project is to decrease the risk of complications like obesity, high cholesterol, or diabetes, and explore associations between bowel and bladder function and nutrition. This study will require 3 in person visits that are about 3 months apart. The total length of the study is about 6 months and includes 3 months of telenutrition counseling.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
96 (estimated)
First submitted
21 Jun 2022
Start date
13 Jun 2022
Primary completion date
1 Mar 2027
Lead sponsor
Santa Clara Valley Health & Hospital System
Diseases
Obesity
NCT number
NCT05468437

What you commit to

  • Study type: Interventional
  • Planned participants: 96
  • From 13 Jun 2022 to the primary completion date, 1 Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Receiving enteral nutrition

Other illness

  • Medical instability (e.g., uncontrolled hypertension, pneumonia, severe pressure injury)
  • Other medical condition requiring a strict specialized diet (e.g., renal failure, diabetes)
  • Current or past diagnosis of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, binge eating disorder)

Lab values

  • HbA1c \>7% (these individuals would need to be treated with metformin or other anti-diabetic medication and the intervention would have to be significantly altered for them)

Other

  • Current self-reported pregnancy
  • Participation in another diet program (e.g., Jenny Craig, Weight Watchers, clinic-based program) and/or participated in another diet program within the past 6 months
  • Individuals without a primary care physician
  • Individuals who are in law enforcement custody

Who the study is looking for

  • Individuals with traumatic SCI
  • At least 1-year post-injury
  • Age 20 years of age or older
  • BMI \> 22 kg/m2 at enrollment
  • Proficiency in English or Spanish
  • Living at home or in a private home setting (i.e., not an extended care facility) in the state of California
  • Able / willing to come to SCVMC for in-person assessments
  • Primarily a wheelchair user (\>40 hours per week)
  • Able to use, or learn how to use, an iPad
  • Possess adequate decision-making capacity to provide independent informed consent

Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Santa Clara Valley Medical Center
Coordinator of this site? Confirm its status
San JoseUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.