RECRUITING

Observation of Environment and Reproductive-Endocrine Effects

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

Background: Endocrine disorders occur when the glands that make hormones do not work properly. Hormones levels that are too high or too low can cause problems such as late or early puberty, irregular periods, and infertility. Environmental factors - including pollution; chemical exposure at home and work; foods; medicines; and sleep habits - may cause problems with the endocrine and reproductive systems. Objective: To learn how environmental factors may affect the endocrine and reproductive systems. Eligibility: Males or females, referring to sex assigned at birth, aged 8 years and older; they must have hypogonadism, infertility, or other reproductive disorders. Design: Adult participants will have 4 to 5 visits in 5 years. Children may have up to 12 visits; they may remain in the study up to the age of 23. Most visits will be less than 3 hours. Participants will be screened. They will have a physical exam. They will have blood and urine tests. They will complete questionnaires; they will answer questions about their diet, health, and other topics. Some may be referred for additional tests, such as imaging scans and semen analysis. Specific tests conducted during study visits will vary, depending on the participant s diagnosis. In addition to repeated blood and urine tests, these may include: Body composition measure: Participants will sit in a pod-shaped machine for about 6 minutes. The machines measures the air inside the capsule to record body fat and breathing volume. Resting energy expenditure test: Participants will lie down with a clear dome placed over their head. They will breathe quietly for 30 minutes. This test measures the number of calories their body burns at rest. ...

Official Title

OBServation of Environment and ReproductiVe Endocrine Effects Study (OBSERVE Study)

Quick Facts

Study Start:2024-07-01
Study Completion:2039-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06280807

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:8 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Male or female, referring to sex assigned at birth (cis gender)
  2. 2. Age \> 8 years and weight \>= 12 kg
  3. 3. A diagnosis of hypogonadism, infertility or other reproductive dysfunction
  4. * Male or female hypogonadism
  5. * Obesity/metabolic syndrome related to hypogonadism.
  6. * Other reproductive dysfunction (e.g., secondary to endocrine dysfunction, thyroid disorders, Cushing syndrome, pharmacotherapy, etc.)
  7. * Premature Ovarian Insufficiency
  8. * Isolated hypogonadotropic hypogonadism
  9. * Polycystic Ovarian Syndrome
  10. * Delayed Puberty
  11. * Precocious puberty
  12. * Perimenopause and post-menopausal states
  13. * Androgen Excess States (Nonclassic Congenital Adrenal Hyperplasia, Extreme hyperinsulism, Idiopathic etc.)
  14. 4. Ability of participant, legal guardian, or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.
  1. 1. A diagnosis of a serious medical disorder such as malignancy or heart disease will be grounds for exclusion at the discretion of the PI or AI.
  2. 2. Inability to follow up with the research study and/or perform study procedures, at the discretion of the PI or AI.
  3. 3. Pregnant participants, less than 18 years of age, for their safety, since there is not a trained doctor on the study to give proper medical care to pregnant individuals less than 18 years of age.

Contacts and Locations

Study Contact

NIEHS Join A Study Recruitment Group
CONTACT
(855) 696-4347
myniehs@nih.gov
Skand Shekhar, M.D.
CONTACT
(301) 451-1866
skand.shekhar@nih.gov

Principal Investigator

Skand Shekhar, M.D.
PRINCIPAL_INVESTIGATOR
National Institute of Environmental Health Sciences (NIEHS)

Study Locations (Sites)

NIEHS Clinical Research Unit (CRU)
Research Triangle Park, North Carolina, 27709
United States

Collaborators and Investigators

Sponsor: National Institute of Environmental Health Sciences (NIEHS)

  • Skand Shekhar, M.D., PRINCIPAL_INVESTIGATOR, National Institute of Environmental Health Sciences (NIEHS)

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 Date2024-07-01
Study Completion Date2039-03-31

Study Record Updates

Study Start Date2024-07-01
Study Completion Date2039-03-31

Terms related to this study

Keywords Provided by Researchers

  • Endocrine
  • Reproductive Disorders
  • Hypothalamic-Pituitary-Gonadal Endocrine Axis

Additional Relevant MeSH Terms

  • Hypogonadism
  • Hypergonadism
  • Precocious Puberty
  • Late Puberty
  • Amenorrhea