The Lake Nona Life Project

October 3, 2023 updated by: University of Central Florida

A Community Epidemiology Study Evaluating the Factors Influencing Overall Health and Wellness

The Lake Nona Life Project aims to examine the health and wellness of participants over the course of multiple years, focusing on the links between health and wellness, longevity, quality of life, and human performance.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The Lake Nona Life Project is a community health and wellness research project of the Lake Nona Institute (LNI), carried out by the Lake Nona Medical City Residents and Partners (the Researchers), and sponsored by Florida Hospital. The project is designed to study patterns, predictors and strategies for improving human health and wellness. Data will be obtained over many years using surveys/interviews, medical tests, and health information from 3rd parties (i.e., health care claims data) obtained with participant permission.

Study Type

Observational

Enrollment (Estimated)

10000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

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.

Eligibility Criteria

Ages Eligible for Study

18 years to 110 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Adults ages 18 and older living and/or working in the Lake Nona Community (proper) of Orlando, Florida.

Description

Inclusion Criteria:

  • 18 years or older
  • Live and/or work in the Lake Nona Community (proper)
  • Able to provide informed consent
  • Able to speak and read English

Exclusion Criteria:

  • Unable to speak or communicate in English
  • Living outside of the LNLP study map
  • Cognitive impairment that would not allow survey completion
  • Unable to speak and read English

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of Life over 10 Years
Time Frame: 20 years
Participants will self report on an Investigator created questionnaire regarding life satisfaction, stress and life events. Responses will be provided on a five point Likert Scale.
20 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Demographics
Time Frame: 20 years
Participants will self report demographic information consisting of questions related to age, gender and race.
20 years
Medical History
Time Frame: 20 years
Participants will self report medical history and chronic conditions.
20 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Central Florida

Collaborators

Lake Nona Institute
DataStat, Inc.
Mytrus, Inc.

Investigators

  • Principal Investigator: Patricia Robinson, Center for CREATION Health Research

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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 Major Dates

Study Start (Actual)

December 31, 2014

Primary Completion (Estimated)

December 31, 2025

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

June 1, 2015

First Submitted That Met QC Criteria

August 24, 2015

First Posted (Estimated)

August 27, 2015

Study Record Updates

Last Update Posted (Actual)

October 6, 2023

Last Update Submitted That Met QC Criteria

October 3, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 1166275

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Quality of Life

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Turkmenistan

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe