- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06377384
FLIGHT Study for Childhood Chronic Illness
September 30, 2025 updated by: Documenting Hope Project
A Pilot and Feasibility Study Focusing on Lifestyle, Environmental Modifications, and Transdisciplinary Clinical Care for Children With Chronic Illness: Protocol for the FLIGHT Study
The FLIGHT study is an open-label, single-arm, pilot and feasibility study of a personalized and multimodality intervention focusing upon modifiable lifestyle factors, environmental modifications, and transdisciplinary clinical care for children with chronic illness.
A mixed methods outcomes evaluation will be performed.
The primary goal of this study is to evaluate the most feasible and promising strategies to inform a more streamlined and scalable intervention in the future.
Up to 14 participants may be enrolled, but fewer are expected to achieve the primary goal of the study.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
2
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
-
Windsor, Connecticut, United States, 06095
- Epidemic Answers
-
-
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
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- At least one guardian must have the ability to read and write English
- Participant and participant's caregiver must reside in the United States and live within the designated recruitment areas
- Verified completion of the CHIRP survey and consent to participate in the FLIGHT Study screening process
- Candidate's diagnosis(es) falls into one or more of the following categories:
- Immune/Autoimmune Conditions (for example: juvenile idiopathic arthritis, juvenile rheumatoid arthritis, asthma, eczema, atopic illness, allergies, Crohn's disease, ulcerative colitis, other gastrointestinal disorders, lupus, other autoimmune conditions)
- Conditions of Metabolic Dysregulation (for example: obesity/type 2 diabetes)
- Mood/Behavioral/Developmental Conditions (for example: autism spectrum disorders, ADHD/ADD, depression, obsessive-compulsive disorder, anxiety)
- Candidate is able to provide sufficient documentation of diagnoses, including validated/standardized diagnostic criteria in current use by specialists for each respective diagnosis, which have been performed by a professional with requisite experience or training
Exclusion Criteria:
- Candidate is a family member or close associate of any employees or board members of Epidemic Answers, members of the FLIGHT Study Team, or any advisors or clinicians associated with the FLIGHT Study
- Candidate is not able to provide documentation for proof of diagnoses
- Diagnosis with a condition that is severe enough to preclude participation in the intensive, multi-modal lifestyle intervention
- Caregiver(s) with health (e.g., serious chronic disease, disability, addiction) or other life circumstances (e.g., lack of transportation, shared custody of child) that preclude full participation in the intensive intervention
- External sources of environmental toxicants to the home or school environment that cannot be modified (e.g., high tension power line directly adjacent to home, coal-fired power plant within a ¼ mile of family's home)
- Inability to control/modify child's diet at daycare or with childcare provider
- Caregiver(s) anticipate a change of geographic location within two years
- Parent or caregiver has explicit belief that child's condition cannot be improved
- Caregiver(s) unwilling to make lifestyle changes, restrict candidate's non-essential technology use. prepare the majority of the family meals at home, replace personal and household products if indicated
- Caregiver(s) unwilling to have the candidate assessed by a team of doctors and/or healthcare practitioners including, but not limited to: physician, chiropractor, acupuncturist, optometrist, nutritionist, or other professionals recommend by the program
- Caregiver(s) unwilling to have the candidate participate in minimally invasive laboratory or non-laboratory assessments
- Caregiver(s) unwilling to have the candidate participate in required periodic video interviews, and other audio-visual documentation
- Candidate is pregnant
- Candidate has been convicted of a felony, is currently on probation, or in a juvenile detention center
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
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: FLIGHT Intervention
|
Personalized and multimodality intervention focusing upon modifiable lifestyle factors, environmental modifications, and transdisciplinary clinical care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total Load Index (TLI)
Time Frame: Baseline and 18 months
|
The TLI is a measure of environmental, chemical, and social stressors that interact to contribute to chronic illness.
There is no numeric score.
|
Baseline and 18 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Health Inventory for Resilience and Prevention (CHIRP)
Time Frame: Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
Comprehensive survey evaluating total load of health stressors and supports influencing children.
There is no numeric score.
|
Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
|
Children's Sleep Habits Questionnaire (CSHQ)
Time Frame: Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
Survey that assesses sleep.
It consists of 35 items scored on a 1-3 point scale, with higher scores indicating worse sleep.
|
Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
|
Vineland Adaptive Behavior Scale
Time Frame: Baseline, 9 months, 18 months
|
Survey assessing developmental and other disorders.
A standard score of 100 is considered average, with scores above 100 indicating strengths in adaptive behavior and scores below 100 indicating areas of difficulty.
|
Baseline, 9 months, 18 months
|
|
Sensory Profile 2
Time Frame: Baseline, 9 months, 18 months
|
Survey assessing child's sensory processing patterns.
There are 86 items.
For each item, a score of 0 indicates that the individual's sensory processing is consistent with age-based norms.
Positive scores suggest that the individual's sensory processing is better than age-based norms, while negative scores indicate that the individual's sensory processing is weaker than age-based norms.
|
Baseline, 9 months, 18 months
|
|
Quick Environmental Exposure and Sensitivity Inventory (QEESI)
Time Frame: Baseline, 9 months, 18 months
|
Survey that assesses environmental toxicants.
The QEESI contains 50 items scored on a 0 to 10 scale with higher scores indicating greater environmental sensitivities.
|
Baseline, 9 months, 18 months
|
|
Hayward Environmental Illness Severity Scale
Time Frame: Baseline, 9 months, 18 months
|
Survey assessing impact of home environment on health.
The survey consists of 22 questions with total score ranges from 0 to 100.
Higher scores indicating greater severity of environmenal sensitivity symptoms.
|
Baseline, 9 months, 18 months
|
|
Parenting Stress Index, 4th edition (PSI-4)
Time Frame: Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
Survey assessing stress among parents.
The PSI-4 contains 120 items with higher scores indicating greater levels of stress.
|
Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
|
Beck Anxiety Inventory (BAI)
Time Frame: Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
Survey assessing anxiety.
The survey contains 21 items with scores ranging from 0 to 63.
Higher scores indicate greater levels of anxiety.
|
Baseline, 3 months, 6 months, 9 months, 12 months, 15 months, 18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 20, 2022
Primary Completion (Actual)
April 30, 2024
Study Completion (Actual)
June 7, 2024
Study Registration Dates
First Submitted
April 17, 2024
First Submitted That Met QC Criteria
April 17, 2024
First Posted (Actual)
April 22, 2024
Study Record Updates
Last Update Posted (Estimated)
October 6, 2025
Last Update Submitted That Met QC Criteria
September 30, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DHP-33-FLIGHT
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
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