RECRUITING

Using a Telehealth and Shared Decision-Making Model to Address Preventative Medicine Strategies Among Communities in Louisiana

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Using a Telehealth and Shared Decision-Making Model to Address Preventative Medicine Strategies Among Communities in Louisiana

Quick Facts

Study Start:2024-01-01
Study Completion:2028-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05676970

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 55 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Adults aged 18 years to 55 years of age
  2. 2. Able to speak English
  3. 3. Currently employed or seeking training in target industries such as: healthcare, education, beauty, hospitality, food (culinary) and industrial plant workers.
  4. 4. Able to use Telehealth technology via tablet, cell phone, or computer
  1. 1. Individuals who are unable to give informed consent.

Contacts and Locations

Study Contact

Sara Al-Dahir, PharmD, PhD
CONTACT
504525766
saaldah@xula.edu
Saba Barri, MPH
CONTACT
5042504537
sbarri@xula.edu

Principal Investigator

Sara Al-Dahir, PhD
PRINCIPAL_INVESTIGATOR
Xavier University of Louisiana.
Klaus Heyer, PhD
PRINCIPAL_INVESTIGATOR
Nunez Community College

Study Locations (Sites)

Xavier University of Louisiana
New Orleans, Louisiana, 70125
United States

Collaborators and Investigators

Sponsor: Xavier University of Louisiana.

  • Sara Al-Dahir, PhD, PRINCIPAL_INVESTIGATOR, Xavier University of Louisiana.
  • Klaus Heyer, PhD, PRINCIPAL_INVESTIGATOR, Nunez Community College

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-01
Study Completion Date2028-12-30

Study Record Updates

Study Start Date2024-01-01
Study Completion Date2028-12-30

Terms related to this study

Keywords Provided by Researchers

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

Additional Relevant MeSH Terms

  • Preventative Medicine