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Chronic Respiratory Disease Participant Engagement Study

NCT07924462, Recruiting, Richmond Research Institute

Trial 8

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleChronic Respiratory Disease Participant Engagement StudyClinicalTrials.gov
NCT numberNCT07924462ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
Enrollment500 participants, estimatedClinicalTrials.gov
Lead sponsorRichmond Research InstituteClinicalTrials.gov
ConditionsInterstitial Lung Disease (ILD), Chronic Respiratory Diseases, Alpha-1 Antitrypsin Deficiency (AATD), Chronic Obstructive Pulmonary Disease (COPD), Asthma, BronchiectasisClinicalTrials.gov
First posted2026-11-09ClinicalTrials.gov
Last updated2026-11-09ClinicalTrials.gov

Registered outcomes 19

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryNumber of patients indicating willingness to be re-contacted for future clinical trialsUntil the end of the study (up to 5 weeks)]ClinicalTrials.gov
PrimaryParticipation feedback questionnaire results using Participant Feedback and Clinical Research Experience QuestionnaireUntil the end of the study (up to 5 weeks)]ClinicalTrials.gov
SecondaryClinical baseline characterisation of medical historyDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of exacerbation historyDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of smoking statusDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of concomitant medications (con-meds)Day 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of respiratory rateDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of body temperatureDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of pulse rateDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of oxygen saturationDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of blood pressureDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of Lung function for FEV1 parameterDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of Lung function for FVC parameterDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of Lung function for FEV1/FVC ratioDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of oxygen useDay 1ClinicalTrials.gov
SecondaryClinical baseline characterisation of bloods including genetic testing where clinically indicated and imaging data where available.Day 1ClinicalTrials.gov
SecondaryNumber and proportion of new diagnoses following assessmentUntil the end of the study (up to 5 weeks)]ClinicalTrials.gov
SecondaryFactors associated with underdiagnosis by exploring differences between patient-reported outcomes and clinical data, including potential variations by age, sex and ethnicityUntil the end of the study (up to 5 weeks)]ClinicalTrials.gov
SecondaryDifferences in patient-reported outcome scores between chronic respiratory disease subgroups using EQ-5D-5L together with the EQ Visual Analogue Scale (EQ VAS)Until the end of the study (up to 5 weeks)]ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)