Recruiting

Vaccine Hesitancy

Sponsor:

Xavier University of Louisiana.

Code:

NCT05676970

Conditions

Preventative Medicine

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Accepted

Interventions

Telehealth: Personalized Preventative Medicine Strategies

TeleHealth: Preventative Medicine Education

Study Details

Brief summary:

This study is a 12-18 month behavioral intervention study to assess the impact of enrolling individuals a clinical pharmacist run Telehealth education focused on wellness and preventive health strategies. Individuals will be randomized to either a wellness education only model focusing on nutrition, diabetes, hyperlipidemia and hypertension or a wellness education model with personalized preventative medicine strategies for the patient. All participants will complete individual and group based interventions. Individuals will be recruited from target work industries such as health workers, teachers aides and the food industry. We are recruiting individuals who come from urban, semi-rural or rural communities or have additional social determinants of health that indicate social vulnerability. The primary outcome is willingness to participate in preventative medicine strategies to prevent development of chronic medical conditions. The secondary outcome is barriers to preventive medicine strategies including for chronic preventable disease such as nutrition, hypertension, hyperlipidemia, diabetes and medication compliance.

Conditions

Preventative Medicine

Study ID

NCT05676970

Start date

Jan 1, 2024

Status verified date

Feb, 2026

Completion date

Dec 30, 2028

Anticipated

Primary completion date

Dec 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Adults aged 18 years to 55 years of age
2. Able to speak English
3. Currently employed or seeking training in target industries such as: healthcare, education, beauty, hospitality, food (culinary) and industrial plant workers.
4. Able to use Telehealth technology via tablet, cell phone, or computer

Exclusion Criteria:

1\. Individuals who are unable to give informed consent.

Study Design

Enrollment

360 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

experimental: Telehealth Arm: Personalized Preventative Medicine Strategies

Individuals in this arm will complete a personalized telehealth interventions that focus on nutrition, work-life balance, medication compliance, herbals, exercise targets hyperlipidemia, diabetes and hypertension around individual risks for development of the disease state. All educations will be completed one-on-one as well as small group.

active comparator: Telehealth Arm: Preventative Medicine Education

Individuals in this arm will complete standardized telehealth interventions that focus on nutrition, work-life balance, mental health, diabetes and hypertension general education. All educations will be completed one-on-one as well as small group.

Interventions

Telehealth: Personalized Preventative Medicine Strategies

Individuals in this arm will complete a personalized telehealth interventions that focus on nutrition, work-life balance, medication compliance, herbals, exercise targets hyperlipidemia, diabetes and hypertension around individual risks for development of the disease state. All educations will be completed one-on-one as well as small group.

TeleHealth: Preventative Medicine Education

Individuals in this arm will complete standardized telehealth interventions that focus on nutrition, work-life balance, mental health, diabetes and hypertension general education. All educations will be completed one-on-one as well as small group.

Primary outcome measure

  • Willingness to participate in preventative medicine screening for Diabetes, Hypertension and Hyperlipidemia [ Time Frame: 12 months, completed year 1 of the study. ]
  • Participating in Screening for DM, hypertension, hyperlipidemia [ Time Frame: Through study completion, on average, 12-18 months ]
  • Willingness to participate in personalized exercise and nutrition goals to prevent chronic disease [ Time Frame: Through study completion, on average, 12-18 months ]
  • Participating in personalized exercise and nutrition goals [ Time Frame: Monthly through study completion, on average, 12-18 months ]
  • Participating in personalized medication compliance for prescription, over the counter, herbals and nutraceuticals related to health promotion [ Time Frame: Monthly through study completion, on average, 12-18 months ]

Central Contacts and Locations

Central contacts

Sara Al-Dahir, PharmD, PhD

5045205766saaldah@xula.edu

Ibrahim Hamed, BSc

5045204537ihamed@xula.edu

Locations

Xavier University of Louisiana

Recruiting

New Orleans, Louisiana, United States, 70125

Contacts

Principal Investigator:

Sara Al-Dahir, PharmD

More Information

Sponsor

Xavier University of Louisiana.

Last update posted

Mar 3, 2026

Last verified

Feb, 2026

Keywords

  • Diabetes
  • Hypertension
  • Hyperlipidemia
  • Medication Compliance
  • Nutrition
  • Exercise

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Xavier University of Louisiana. on 2026-03-03.