Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Dietary approaches to improve asthma control

Official title: Individualized Nutrition to Help Asthmatics Improve Lung Function and Energetics (INHALE)

Run by Pennington Biomedical Research Center · NCT06151405 · Data updated 2026-11-12

This study is testing whether different diets can help adults with asthma breathe better and manage their symptoms.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment15 (estimated)
SponsorPennington Biomedical Research Center
Academic / other
Locations1 site (Baton Rouge, Louisiana)
StatusRecruiting
StartedJuly 17, 2024
Main results expectedDecember 31, 2026
Study endsMarch 1, 2027
Registry record updatedSeptember 19, 2024
Trial IDNCT06151405 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18-65 with partly controlled or uncontrolled asthma and a stable medication regimen.

Probably not a fit

Patients with diabetes, significant comorbidities, or those with dietary restrictions incompatible with the study diets may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot trial investigates the impact of three different dietary interventions on asthma control and lung function in adults with asthma. Participants will be randomly assigned to follow a DGA Diet, MCT Diet, or KETO Diet for seven days, with a washout period in between each diet. The study aims to assess changes in asthma control and lung function after each dietary phase, while also exploring factors that may influence dietary response. A total of 15 adults will be recruited for this crossover design trial.

Why it matters

Potential benefit: If successful, this study could provide new dietary strategies to improve asthma management and enhance lung function.

How similar studies have gone: While dietary interventions in asthma management are being explored, this specific crossover approach is relatively novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age: 18-65 years
* BMI: 18.5 - 29.99 kg/m2
* asthma diagnosed by medical specialist (confirmed in medical history)
* partly controlled or uncontrolled asthma by Asthma Control Test score ≤22
* owns a device compatible with ZEPHYRx platform
* stable asthma medication use (no change in the past 2 months).

Exclusion Criteria:

* Diabetes or using diabetes medications that may lower blood glucose levels
* point of care fasting blood glucose ≥126 mg/dl or triglycerides ≥400 mg/dl
* current smoking or smoking history of greater than 10 pack-years
* other significant respiratory or cardiac disease or the presence of clinically important comorbidities, e.g., COPD, renal failure, liver disease; uncontrolled hypertension defined as systolic blood pressure ≥160 mm/Hg, or diastolic blood pressure ≥100 mm/Hg
* pregnant or nursing women
* food preferences or allergies inconsistent with study diet capabilities
* noncompliance with lead-in period requirements.

Where it's running

  • Pennington Biomedical Research Center
    Baton Rouge, Louisiana, United States
    Recruiting

Study contacts

  • Principal investigator: Jacob T Mey, PhD, RD — Pennington Biomedical Research Center
  • Study coordinator: Jacob T Mey, PhD, RD
  • Email: jacob.mey@pbrc.edu
  • Phone: 225-763-2644

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.