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Registry for Asthma Characterization and Recruitment 2 (RACR2)

Registry for Asthma Characterization and Recruitment 2 (ICAC-25)

There is a need for people to take part in research studies to learn more about diseases and how to treat them. The Registry for Asthma Characterization and Recruitment 2 (RACR2) will create a database of participants with asthma and nasal allergies, or risk factors for these conditions, who are potentially eligible for future Inner City Asthma Consortium (ICAC) trials. The registry database will include assessments of various asthma and allergy characteristics to achieve a more efficient, selective recruitment of these participants for other protocols.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

The overall goal of the Registry for Asthma Characterization and Recruitment 2 (RACR2) is to create a database of participants who are potentially eligible for future Inner City Asthma Consortium (ICAC) clinical research studies. The registry will provide an avenue to assess various asthma and allergy characteristics, which will result in more efficient recruitment for current and future ICAC protocols.

Potential participants will be recruited via telephone or in person. Those deemed potentially eligible for a current protocol or protocol in development may be invited to the clinic for further data collection and assessments. This registry allows flexibility in selecting the eligibility criteria and data collection to match planned or upcoming ICAC protocols. At each stage of data collection, participants may be discontinued, put on hold, or invited to participate in further screening activities, depending on the likelihood that they will qualify for a future protocol. Participants may opt to withdraw their information or discontinue from the registry at any time, in person, by telephone, or in writing.

Type d'étude

Observationnel

Inscription (Réel)

1384

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Colorado
      • Aurora, Colorado, États-Unis, 80045
        • Children's Hospital Colorado
    • District of Columbia
      • Washington, District of Columbia, États-Unis, 20010
        • Children's National Medical Center
    • Illinois
      • Chicago, Illinois, États-Unis, 60611
        • Ann and Robert Lurie Children's Hospital of Chicago
    • Maryland
      • Baltimore, Maryland, États-Unis, 21205
        • Johns Hopkins University
    • Massachusetts
      • Boston, Massachusetts, États-Unis, 02118
        • Boston Medical Center
    • Michigan
      • Detroit, Michigan, États-Unis, 48202
        • Henry Ford Health System
    • Missouri
      • Saint Louis, Missouri, États-Unis, 63110
        • St. Louis Children's Hospital
    • New York
      • New York, New York, États-Unis, 10032
        • Columbia University Medical Center
    • Ohio
      • Cincinnati, Ohio, États-Unis, 452229
        • Cincinnati Children's Hospital
    • Texas
      • Dallas, Texas, États-Unis, 75390
        • University of Texas Southwestern Medical School

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

1 an à 55 ans (Enfant, Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

Subjects who reside within the metropolitan statistical area of the clinical site and have clinician-diagnosed asthma, current symptoms of asthma, or risk factors for development of asthma. The population may at times include participants without asthma, atopy, and rhinitis.

La description

Inclusion Criteria:

Eligibility criteria vary depending on recruitment needs for future ICAC protocols. Participants with asthma and participants without asthma, atopy, and rhinitis may be recruited at the same time or different times, depending on recruitment needs.

Certain characteristics or groups of characteristics within each criterion may be selected for periods of time across clinical sites or at each individually participating clinical site. For example, over a 6-month period, the Consortium could decide to recruit children aged 6 through 12 years with diagnosed asthma who have asthma symptoms, have a history of an asthma exacerbation, and reside in prespecified census tracts within the metropolitan statistical area. During selective recruitment periods, individuals who meet broader criteria may or may not be enrolled at the discretion of the Consortium.

  1. All participants must resides within the metropolitan statistical area that includes the clinical site.
  2. Participants with asthma are defined by having evidence of asthma. Evidence of asthma is defined by meeting at least one of the following criteria:

    • Clinician-diagnosed asthma
    • Asthma symptoms, history of an asthma exacerbation, or current use of asthma medication(s)
    • Recurrent wheezing
    • Wheezing apart from a cold

    At times of selective recruitment, participants with asthma may be required to meet more selective criteria above and may be required to meet one or more of the criteria in risk factors for asthma. Evidence of risk factors for asthma is defined by meeting at least one of the following criteria:

    • Parental history of asthma
    • Eczema or atopic dermatitis
    • Reported allergies to pets, food, indoor allergens, or outdoor allergens
    • Allergic sensitization by results of allergy skin testing or results of serum immunoglobulin E (IgE) testing
    • Rhinitis
  3. Participants without asthma, atopy, and rhinitis must meet all of the following:

    • Negative history of an asthma diagnosis by a clinician
    • Negative history of a diagnosis of atopic dermatitis or eczema by a clinician
    • Negative history of a rhinitis diagnosis by a clinician
    • A forced expiratory volume at 1 second (FEV1) >= 5% predicted
    • Negative prick skin-tests to any of a panel of indoor and outdoor allergens
    • No current asthma as determined by the appropriate case report form
    • No current chronic rhinitis/sinusitis as determined by the appropriate case report form

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from enrollment:

  1. Has any of the following chronic medical conditions: cardiac condition requiring daily medication, seizure disorder requiring daily medication, obvious severe mental retardation that prevents the participant from answering questions or following instructions, cystic fibrosis, immune deficiency, type 1 diabetes, allergic bronchopulmonary aspergillosis, or any other chronic medical condition at the discretion of the registry clinician
  2. Does not primarily speak English (or Spanish at clinical sites with Spanish-speaking staff)
  3. Has a primary caretaker who does not speak English (or Spanish at clinical sites with Spanish-speaking staff; not applicable if participant is able to provide consent)
  4. Is a foster child (not applicable if participant is able to provide consent)
  5. Is unwilling to sign the written informed consent form if of age, or parent/legal guardian is unwilling to sign the written informed consent if participant is not of age
  6. Is unwilling to sign the assent form, if age appropriate

Participants who are pregnant will not be excluded or discontinued from RACR2 but will not undergo any procedures that are prohibited during pregnancy.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Number of participants with asthma and allergy characteristics
Délai: Year 7
Characteristics of the participants enrolled in the registry will be assessed on a periodic basis (descriptive summary of diagnosis and parameters associated with the former).
Year 7

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Jacqueline Pongracic, M.D., Ann & Robert H Lurie Children's Hospital of Chicago
  • Chercheur principal: Edward M. Zoratti, M.D., Henry Ford Hospital

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

14 avril 2015

Achèvement primaire (Réel)

13 mars 2020

Achèvement de l'étude (Réel)

13 mars 2020

Dates d'inscription aux études

Première soumission

23 juillet 2015

Première soumission répondant aux critères de contrôle qualité

30 juillet 2015

Première publication (Estimation)

31 juillet 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

25 janvier 2021

Dernière mise à jour soumise répondant aux critères de contrôle qualité

22 janvier 2021

Dernière vérification

1 janvier 2021

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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