RECRUITING

Wearable Devices and Biomarkers Project (Healthiomics)

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 purpose of this study is to collect clinical data, biological specimens (e.g., blood, tumor, cerebrospinal fluid, urine sample, etc.), and digital health data from patients with tumors, cancer and/or neurological disorders in order to perform research studies that could advance patient care. By collecting these specimens, the investigators plan to create and maintain a biorepository to make data and specimens available to collaborating investigators performing research to discover predictive biomarkers, patterns of care, and personalized treatments that could directly improve the care of our patients through focused proof-of-concept clinical trials.

Official Title

Study of Clinical Biomarkers in Human Health and Disease (Healthiomics)

Quick Facts

Study Start:2021-10-11
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05106725

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. * Participant or participant's legally authorized representative has the ability to understand and the willingness to provide a signed and dated informed consent form.
  2. * Participant is ≥ 18 years of age.
  3. * Participant had/has a scheduled appointment with oncology or neurosciences services at the participating medical and surgical facility.
  4. * Participant is characterized by at least one of the following criteria:
  5. 1. Has a neurological complication from any type of cancer, or is under evaluation for a possible cancer diagnosis or neurologic complication. Participant may be newly diagnosed, in relapse, or be free of disease at the time of recruitment. Participant without a confirmed cancer diagnosis is eligible.; OR
  6. 2. Has a neurological disorder, or is under evaluation for a possible diagnosis of a neurological disorder; OR
  7. 3. Does not meet the characteristic of either a. or b. above. This participant would be considered a "healthy control" for cancer and neurological disorders.
  1. * Participant or participant's legally authorized representative is unable to provide informed consent.

Contacts and Locations

Study Contact

Amanda Wilburn
CONTACT
8588002873
awilburn@curescience.orgg

Principal Investigator

Feng Lin, MD PhD
PRINCIPAL_INVESTIGATOR
CureScience

Study Locations (Sites)

CureScience Institute
San Diego, California, 92121
United States

Collaborators and Investigators

Sponsor: CureScience

  • Feng Lin, MD PhD, PRINCIPAL_INVESTIGATOR, CureScience

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 Date2021-10-11
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2021-10-11
Study Completion Date2025-12-31

Terms related to this study

Keywords Provided by Researchers

  • wearables
  • digital health
  • biospecimens

Additional Relevant MeSH Terms

  • Brain Cancer
  • Neurological Disorder
  • Neurological Cancer