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RecruitingNCT05965947HOMEUpdated Dec 9, 2024

The HOME Study (Healthy Options Made Easy): Telehealth Nutrition Sessions for People Living With Brain Injury

An interventional study of Medical Nutrition Therapy in Brain Injuries, sponsored by University of Alabama, Tuscaloosa. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-12-09.

Sponsored by University of Alabama, Tuscaloosa · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Oct 2025, 1 year ago, but the record still lists the study as recruiting.
  • Started Jun 2023; still recruiting 3 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
134
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Brain injury is a leading cause of disability in the United States. When survivors of brain injury recover from the initial injury and return home to live in the community, they often face chronic health conditions that warrant nutrition therapy, such as diabetes, high blood pressure, high cholesterol, and overweight and obesity. Typically, these individuals do not receive nutrition counseling.

Thus, the purpose of this clinical trial is to compare changes in diet quality between community-dwelling individuals with a history of brain injury who receive three individualized nutrition therapy sessions versus handouts only.

Our research question is:

Can nutrition counseling improve dietary intake among this population?

Participants will complete a survey, participate in three days of dietary recalls via Zoom or telephone, and receive either three individualized nutrition counseling sessions with a Registered Dietitian or standard of care (handouts).

Researchers will compare the diets of the recipients of the nutrition counseling to a control group who receives nutrition handouts to see if nutrition sessions with a Registered Dietitian improve dietary intake.

Read the detailed description

The purpose of this study is to evaluate the impact of providing nutrition therapy on diet among a cohort of community-dwelling individuals with a history of brain injury.

In this pre/post study, 134 participants with brain injury will be recruited and randomized to the control or intervention group. All participants will complete a standard set of nutrition-related questionnaires to assess weight status, co-morbid conditions, food security, stressors, stress-related eating, eating behaviors, and diet quality.

The control group will receive a packet of nutrition education materials. The intervention group will receive the packet and one-on-one nutrition counseling with a Registered Dietitian.

Follow-up data collection will include repeating the dietary recalls and questionnaires. This will allow for an evaluation of the impact of nutrition therapy on diet quality among community-dwelling individuals with brain injury.

Aim: Evaluate the effectiveness of providing nutrition therapy on diet quality and stress-related eating among a cohort of community-dwelling individuals with brain injury

  • Ho: Individuals who receive three nutrition therapy sessions with a Registered Dietitian will have greater increases in Healthy Eating Index (HEI) scores than those who receive only handouts (current practice).
02

Conditions studied

  • Brain Injuries

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Keywords

  • brain injury
  • Medical Nutrition Therapy
  • Registered Dietitian
  • diet quality
  • Healthy Eating Index
03

In context

Brain Injuries

2,125 studies on the registry are indexed under Brain Injuries; 384 are open to participants now.

This study's planned enrollment of 134 is above the median of 48 across 1,341 interventional studies indexed under Brain Injuries.

Browse Brain Injuries studies →

Lead sponsor

University of Alabama, Tuscaloosa is the lead sponsor of 42 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • At least 18 years of age
  • History of brain injury
  • Live in Alabama
  • Live at home in the community
  • Have internet access to join Zoom sessions

Exclusion criteria

Exclusion Criteria:

  • Under 18 years of age
  • No history of brain injury
  • Lives outside of Alabama
  • Currently in a hospital, rehabilitation facility, group home, or other location other than 'home'
  • Pregnant or breastfeeding
  • Not able/willing to participate based on the Decision-Making Capacity Assessment
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
134 participants (estimated)

Study arms

  • Experimental
    Medical Nutrition Therapy

    The intervention group will be scheduled for three one-on-one sessions with a Registered Dietitian, where they will receive nutrition education and counseling. Sessions with the Registered Dietitian will include a review of the client's nutrition assessment data, development of problem list with the client, nutrition diagnosis, assessment of motivation to change, a discussion of barriers and facilitators, an intervention plan, goal setting, and monitoring and evaluation. Because individuals with brain injury may not do their own grocery shopping and meal preparation, caregivers will be encouraged to attend sessions. Checklists will be used to ensure treatment fidelity across participants and nutrition sessions. Sessions will be conducted by telehealth and will be recorded for fidelity checks and ongoing research team training. Sessions will be scheduled approximately 2 weeks apart.

    Behavioral: Medical Nutrition Therapy

  • No intervention
    Nutrition Handout Packet

    The control group will receive a packet of nutrition education handouts from the MyPlate program found at USDA.gov. The handouts are publicly available and represent nutrition information that could be readily accessed by individuals who want to change their dietary habits, but do not have access to services from a Registered Dietitian.

Interventions

  • BehavioralMedical Nutrition Therapy

    One-on-one nutrition assessment, education, and counseling with a Registered Dietitian.

    Also known as: nutrition therapy, nutrition counseling, nutrition education

06

What researchers measure

Primary outcomes

  1. Change in Diet Quality

    Diet quality is measured using the Healthy Eating Index Score, which ranges from 0-100. Higher scores indicate better diet quality. The score will be calculated at baseline and approximately 6 weeks later, and these timepoints will be used to calculate the change in diet quality over the study duration.

    Time frame: Baseline and approximately 6 weeks later

07

Study locations

1 of 1 sites recruiting
  • The University of Alabama
    Tuscaloosa, Alabama 35487, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05965947
Lead sponsor
University of Alabama, Tuscaloosa
Collaborators
Academy of Nutrition and Dietetics
Responsible party
Sponsor
First posted
Jul 28, 2023
Start date
Jun 12, 2023
Primary completion
Oct 1, 2025 (estimated)
Completion
Oct 31, 2025 (estimated)
Last update
Dec 9, 2024

Study contacts

Joy W Douglas, PhD
Contact
jdouglas@ches.ua.edu
2053488044
Linda L Knol, PhD
Contact
lknol@ches.ua.edu
2053488129
Joy W Douglas, PhD
principal investigator · The University of Alabama
Linda L Knol, PhD
principal investigator · The University of Alabama

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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