Recruiting

Observational Study

Sponsor:

Emory University

Code:

NCT04002882

Conditions

Cystic Fibrosis

Eligibility Criteria

Sex: All

Age: 16+

Healthy Volunteers: Accepted

Study Details

Brief summary:

Nutrition and body composition, the amount of muscle and fat in the body, has a role in overall health. This study wants to learn more about how nutrition and body composition affects health outcomes like glucose tolerance and lung function in patients with cystic fibrosis (CF) who are ages 16-30 years old. 60 adolescents and young adults with CF will be recruited, and 30 volunteers without cystic fibrosis. A total of 40 of these study participants with CF will be asked to return for annual study visits for 2 years after the first visit.

The long-term goal of this study is to use the information collected to make decisions about future nutrition monitoring and interventions which help maintain optimal health for individuals with CF.

Conditions

Cystic Fibrosis

Study ID

NCT04002882

Start date

Jul 8, 2019

Status verified date

May, 2026

Completion date

May, 2027

Anticipated

Primary completion date

May, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 16+

Healthy Volunteers: Accepted

Inclusion Criteria:

CF inclusion criteria

1. confirmed CF diagnosis based on sweat testing by pilocarpine iontophoresis and/or CFTR genotyping with two disease causing mutations
2. be aged ≥ 16 yrs
3. clinically stable, defined as no changes in medical regimen (including medications) for at least 21 days prior to study visit
4. participation in the CFF Patient Registry

Longitudinal study inclusion:

CF participants who have normal glucose tolerance results after their initial study oral glucose tolerance test (OGTT).

Healthy controls inclusion criteria:

1. male or female ages 16 years and older
2. clinically stable. Healthy controls will be recruited who are similar in age, gender, and BMI as the participants with CF.

Exclusion Criteria:

CF exclusion criteria:

1. diagnosis of CF-related diabetes (CFRD)
2. nocturnal tube feeds
3. life expectancy <6 months
4. history of or on waiting list for lung transplant
5. un-removable metal that is incompatible with MRI
6. inability or unwillingness to perform major study activities (OGTT, DEXA, MRI) due to claustrophobia, fear of blood draw, or other reasons
7. current pregnancy or lactation
8. study visit falls between window of 1 week to 8 weeks of initiation of CFTR modulator
9. use of chronic oral corticosteroids,
10. in the opinion of the CF Care Team or study physician, participant should not participate in the study, or
11. inability to provide informed consent or assent.

Healthy controls exclusion criteria:

1. malignant neoplasm (other than localized basal cell cancer of the skin) during the previous 5 years
2. respiratory (including asthma), endocrine (including diabetes), autoimmune, or other chronic disease
3. HIV or other chronic infection
4. current use of any medications to treat an acute or chronic disease or illness (anti-depressants, anti-anxiety medications are acceptable),
5. acute illness within the past 3 weeks
6. intravenous or oral antibiotics or use of systemic corticosteroids within the past 3 weeks
7. inability or unwillingness to perform major study activities due to claustrophobia, fear of blood draw, or other reasons
8. current pregnancy or lactation, or
9. inability to provide informed consent or assent.

Study Design

Enrollment

90 participants

Anticipated

Interventions and Outcome Measures

Arms

Subjects with Cystic Fibrosis

n=60 patients with CF ages 16-30

Healthy Controls

n=30 healthy controls matched to participants with CF for age, sex, BMI, and race.

Primary outcome measure

  • Change in Visceral Adipose Tissue volume (VAT) by Magnetic Resonance Imaging (MRI) [ Time Frame: Baseline, 1 year, 2 year ]
  • Change in Disposition Index [ Time Frame: Baseline, 1 year, 2 year ]
  • Change in Forced Expiratory Volume in the first second (FEV1%) [ Time Frame: Baseline, 1 year, 2 year ]

Central Contacts and Locations

Locations

Emory University/Children's Hospital of Atlanta (CHOA)

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

More Information

Sponsor

Emory University

Last update posted

May 18, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-16. This information was provided to ClinicalTrials.gov by Emory University on 2026-05-18. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.