Improving Dietary Quality and Social Engagement Through a Virtual Nutrition and Teaching Kitchen Intervention Among Older Veterans With Impaired Mobility

Not Applicable

Not yet recruiting

• Conditions: Impaired Mobility

• Registration Number: NCT06726083
• Lead Sponsor: VA Office of Research and Development

Brief Summary

Compared to non-Veterans, Veterans demonstrate an increased risk for obesity and multimorbidity. Thus, interventions to improve overall health are warranted in this population. Healthy diets that include fruits and vegetables are linked to a reduced risk of chronic disease including mobility disability, and are associated with higher muscle mass, strength and physical performance potentially slowing further disability progression later in life. The investigators will determine if a three-month virtual group nutrition intervention paired with produce delivery and virtual teaching kitchen cooking demonstrations tailored for older Veterans with impaired mobility will improve diet, health-related quality of life and muscle strength.

Detailed Description

There are \>8 million older Veterans (\>65 years) in the United States, and nearly half of them self-report having a disability such as impaired mobility that impacts their ability to perform self-care. Among older Veterans with mobility disability, common self-care tasks like food shopping, meal preparation, and cooking are barriers to consuming a healthy diet, resulting in poor dietary intake. Poor dietary intake contributes to chronic disease risk and loss of muscle mass and strength, consequently limiting function and increasing immobility. Teaching older Veterans with impaired mobility how to overcome barriers limiting these diet-related self-care tasks provides an opportunity to significantly impact this group's dietary intake. Lack of social support has also been associated with negative health outcomes and poor nutritional intake; thus, effective, age-friendly intervention strategies to improve dietary quality as a strategy to delay further progression of disability and maintain functional independence among this population are needed.

In this randomized controlled trial, the investigators will determine if a 3-month virtual group nutrition intervention paired with produce delivery and virtual teaching kitchen cooking demonstrations tailored for older Veterans will improve diet and functional mobility. The overarching hypothesis is that virtual group nutrition education classes and cooking demos, personalized to include considerations of this population's physical limitations, age-related taste changes and technological barriers, will result in favorable improvements in dietary quality and functional mobility while promoting social interaction.

Specific Aim 1: determine the impact of the virtual intervention paired with produce delivery and virtual cooking demonstrations on objective measures of diet quality compared to contact control among a diverse sample of older Veterans with impaired mobility. Additionally, the investigators will assess the sustained effects of the program on dietary quality at a 6-month follow-up, 3-months after the virtual intervention ends. If no treatment effects are observed at the end of the 3-month intervention, the investigators will explore reasons why the intervention was ineffective.

Specific Aim 2: determine the impact of the 3-month virtual nutrition intervention on measures of social isolation, health-related quality of life and mental health using validated questionnaires.

Specific Aim 3: determine associations with changes in dietary quality and frailty-related physical function outcomes and body composition among those who benefit from a virtual nutrition education and cooking program.

Study Timeline

• Status Verified: 2024-12
• Study First Submitted: 2024-12-05
• Study First Submitted QC: 2024-12-05
• Last Update Submitted: 2024-12-05
• Study First Posted: 2024-12-10
• Last Update Posted: 2024-12-10
• Study Start: 2025-10-01
• Primary Completion: 2029-09-30
• Study Completion: 2029-09-30

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 180

Inclusion Criteria

• Veterans >65 years with reduced gait speed (gait speed <1.0 m/s) or elevated four square step test
• use of an assistive device who also indicate that they would like to improve their eating habits, defined by response of <3 on a scale of 1 to 5 to the question, 'Do you consider your eating habits to be healthy'

Exclusion Criteria

• uncontrolled diabetes mellitus or chronic kidney disease
• contraindications to a nutrition intervention including physician prescribed diet (e.g. renal diet)
• dementia (on medical record review or a mini-mental status exam score <24)
• currently participating in a diet or weight loss intervention
• behavior that prevents group interaction

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Diet quality	3 month and 6 month compared to baseline	Habitual dietary intake will be assessed using three 24-h recalls via the online Automated Self-Administered 24-hour (ASA24) Dietary Assessment Tool, version (2022), developed by the National Cancer Institute, Bethesda, MD. The dietary recalls will be used to calculate diet quality using the HEI; scores range from 0 to 100; higher scores indicate better adherence to the Dietary Guidelines for Americans.
Social Isolation	3 month and 6 month compared to baseline	The Lubben Social Network Scale, is a 12-item scale to assess self-reported social engagement including family and friends (Cronbach's =0.70). The total score is calculated by finding the sum of the all items. The score ranges between 0 and 60, with a higher score indicating more social engagement. The UCLA Loneliness Scale is a 20-item scale to measure subjective feelings of loneliness \& social isolation (Cronbach's 0.89\<0.94). Using a 4-point rating scale (1= never; 4 = always), participants answer 20 questions, such as "How often do you feel left out?" and "How often do you feel part of a group of friends?" Researchers later reverse-code the positively worded items so that high values mean more loneliness, and then calculate a score for each respondent by averaging their ratings. Both measures are included because they assess complementary but separate constructs

Secondary Outcome Measures

Name	Time	Method
Health-related Quality of Life	3 month and 6 month compared to baseline	The PROMIS Global Health (v1.2) consist of 10 items on a 5-pt Likert scale to measure an individual's physical (GPH) and mental health (GMH). The GPH score comprises 4 items on physical health, physical functioning, pain intensity, and fatigue. The GMH score includes 4 items on overall HRQoL, mental health, satisfaction with social activities/relationships, \& emotional problems. Higher scores indicate better HRQoL.
Body Composition	3 month	Total and regional percentage body fat, absolute fat mass and fat-free mass will be measured using dual energy X-ray absorptiometry (DEXA).
Modified Physical Performance Test (MPPT)	3 month and 6 month compared to baseline	The MPPT is a nine-item standardized test used to identify frailty and mobility dysfunction in older individuals. It scores individuals on the time it takes to complete such tasks as donning and doffing a coat, picking a penny from the ground, and ascending the stairs. These scores are then summed out of 36 and scores of less than 32 indicate at least mild frailty.
Functional Gait Assessment (FGA)	3 month and 6 month compared to baseline	The FGA is a 10-item clinical gait test that is based on the dynamic gait index (DGI). It tests higher level dynamic gait activities that are part of daily functional mobility such as turning safely and ambulating backwards. Total scores ranging from 0 to 30 and scores below 22 are predictive of future falls.
Falls-Efficacy Scale-International (FES-I)	3 month and 6 month compared to baseline	The FES-I is a 16-item self-reported tool that measures fear of falling when completing routine activities such as preparing a meal, going shopping, getting dressed, visiting with friends and family, and reaching up or bending down. The level of concern is measured on a four-point Likert scale (1=not at all concerned to 4=very concerned). It is scored from 16-64 points (high fear of falling \>23 points)

Trial Locations

Locations (1)

Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD; 🇺🇸 Baltimore, Maryland, United States