Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05251402 · ClinicalTrials.gov registry record · Phase 2

Addressing Quality of Life, Clinical Outcomes, and Mechanisms in Uncontrolled Asthma Following the DASH Dietary Pattern

A Phase 2 study of Asthma, sponsored by University of Illinois at Chicago.

Active
Registry status
Phase 2
Development phase
323
Enrollment target
2
Study locations

NCT05251402: Active Phase 2 study of Asthma, sponsored by University of Illinois at Chicago.

NCT05251402 is a Phase 2 study of Asthma that is active but no longer recruiting, run by University of Illinois at Chicago. The registered enrollment target is 323 participants, below the 1,562-participant average among 374 other Asthma trials with a reported enrollment target (79% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05251402, a Phase 2 study of Asthma, is active but no longer recruiting, sponsored by University of Illinois at Chicago.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
323 participants
Enrollment target
2
Study locations

Study Summary

The goal of the ALOHA trial is to investigate the efficacy of improved diet quality following a DASH behavioral intervention that has shown promising results in adults with uncontrolled asthma. DASH stands for Dietary Approaches to Stop Hypertension. This healthy diet is known to help people with high blood pressure manage their health. But physicians do not know if the DASH diet can also benefit patients with uncontrolled asthma. Researchers in the ALOHA study are trying to find out the answer to this important question. Researchers at UIC are studying how 2 asthma care programs compare in terms of helping adults with uncontrolled asthma to improve their quality of life. Researchers also want to learn what might explain the differences in patient outcomes that they may see between the 2 programs. The primary outcome will be asthma-specific quality of life. If the DASH behavioral intervention is found to benefit people with uncontrolled asthma, it would provide a practical, safe, and acceptable public-health intervention in the form of dietary modification to reduce the burden of asthma.

Primary Outcome

The 15-item Juniper Mini Asthma-Specific Quality of Life Questionnaire (AQLQ) has been shown to have excellent reliability and responsiveness to change in asthma control. It consists of 5 items on symptoms, 4 items on activity limitations, 3 items on emotional function, and 3 items concerning environmental stimuli. Each item is rated on a scale from 1=maximum impairment to 7=no impairment over the last 2 weeks. The overall AQLQ score is an average of the item scores equally weighted. The primary

Conditions Studied

Interventions

  • BEHAVIORAL Group A - Patient Education
  • BEHAVIORAL Group B - Patient Education with Nutrition Counseling

Study Locations (2)

Illinois

  • Department of Medicine - Chicago
  • UIC CCTS Clinical Research Center - Chicago

Trial Details

FieldValue
Enrollment Target 323 participants
Start Date 2022-03-09
Est. Completion 2026-09-01
Phase Phase 2
University of Illinois at Chicago

430 total trials

What the registry record for NCT05251402 still lists

NCT05251402 is an interventional study that assigns participants to a tested intervention. The registered 323 participants enrollment target is mid-sized for trials with a published cap, below the 1,562-participant average among 374 other Asthma trials with a reported enrollment target (79% lower).

The record links to 1 condition, with Asthma appearing as the primary indexed condition, and to 2 interventions - of which Group A - Patient Education is the first listed.

NCT05251402 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT05251402 about?

NCT05251402 is a clinical study titled "Addressing Quality of Life, Clinical Outcomes, and Mechanisms in Uncontrolled Asthma Following the DASH Dietary Pattern". The goal of the ALOHA trial is to investigate the efficacy of improved diet quality following a DASH behavioral intervention that has shown promising results in adults with uncontrolled asthma. DASH stands for Dietary Approaches to Stop Hypertension. This healthy diet is known to help people with hi...

What is the current status of trial NCT05251402?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 323 participants. The study started on 2022-03-09. Estimated completion is 2026-09-01.

What conditions does trial NCT05251402 study?

This clinical trial studies the following conditions: Asthma.

What interventions are being tested in trial NCT05251402?

The interventions under investigation include: Group A - Patient Education (BEHAVIORAL), Group B - Patient Education with Nutrition Counseling (BEHAVIORAL).

Who is sponsoring clinical trial NCT05251402?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05251402 being conducted?

This trial has 2 study locations across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Asthma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05251402's enrollment target sits among peer trials

323 116th of 374 higher than 259 of 374 other Asthma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Asthma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04164173 · 324 participants · NA

    Hyperinflation Respiratory Therapies in Cardiac Surgery Patients

  • NCT04708054 · 324 participants · Phase 2

    Venetoclax to Improve Outcomes of Fractionated Busulfan Regimen in Patients With High-Risk AML and MDS

  • NCT05261399 · 324 participants · Phase 3

    Savolitinib Plus Osimertinib Versus Platinum-based Doublet Chemotherapy in Participants With Non-Small Cell Lung Cancer Who Have Progressed on Osimertinib Treatment

  • NCT05353322 · 324 participants · NA

    Breaking up Prolonged Sedentary Behavior to Improve Cardiometabolic Health

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05251402, the US trial registry maintained by the National Library of Medicine. NCT05251402 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.