RECRUITING

Investigating Health Impacts of Exposure to Harmful Algal Blooms

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

The goals of this project are to study the biological effects of environmental toxins (ET), in particular aquatic toxins such as brevetoxins (PbTx) and microcystin or their metabolites. This study is designed to examine the effects of the body from harmful algae blooms (HAB) as well as possibility of an association between exposure to the marine toxin, brevetoxin (PbTx), which is released from K. brevis during the red tide bloom, and the prevalence of neurological illnesses.

Official Title

Investigating Health Impacts of Exposure to Harmful Algal Blooms

Quick Facts

Study Start:2024-10-14
Study Completion:2030-10-14
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06883227

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Subject should be able to provide written informed consent.
  2. 2. Adult aged 18 or older.
  3. 3. Resident (temporary or permanent) of one of the following five southwest Florida counties (Lee, Collier, Charlotte, Sarasota, or Manatee).
  4. 4. Any race or ethnicity.
  5. 5. Willing to return for at least a total of four study visits and participate in all required procedures for the duration of the study.
  1. 1. Inability to speak or write in English.
  2. 2. Any medical condition for which the study investigator believes enrollment is medically inappropriate.
  3. 3. Unwilling/unable to provide biological samples or poor venous access.

Contacts and Locations

Study Contact

Dakota Helgager Clinical Research Site Coordinator, Bachelor's
CONTACT
9412568010
redtide@roskampclinic.org
Ayse Cemek Clinical Research Coordinator, Bachelors
CONTACT
9412568010
redtide@roskampclinic.org

Principal Investigator

Laila Abdullah Principal Investigator, Ph.D
PRINCIPAL_INVESTIGATOR
The Roskamp Institute

Study Locations (Sites)

The Roskamp Institute
Sarasota, Florida, 34232
United States

Collaborators and Investigators

Sponsor: Roskamp Institute Inc.

  • Laila Abdullah Principal Investigator, Ph.D, PRINCIPAL_INVESTIGATOR, The Roskamp Institute

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 Date2024-10-14
Study Completion Date2030-10-14

Study Record Updates

Study Start Date2024-10-14
Study Completion Date2030-10-14

Terms related to this study

Keywords Provided by Researchers

  • Brain fog
  • Red Tide
  • respiratory
  • coughing
  • neurotoxin
  • beach
  • florida

Additional Relevant MeSH Terms

  • Red Tide
  • Neurologic Disorder
  • Florida