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Pulmonary Fibrosis Contact Registry

This study is currently recruiting participants.
Verified August 2013 by Jeff Swigris, National Jewish Health
Sponsor:
ClinicalTrials.gov Identifier:
NCT01935726
First Posted: September 5, 2013
Last Update Posted: November 18, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborators:
Pulmonary Fibrosis Foundation
Patient-Centered Outcomes Research Institute
Information provided by (Responsible Party):
Jeff Swigris, National Jewish Health
August 31, 2013
September 5, 2013
November 18, 2014
August 2013
January 2040   (Final data collection date for primary outcome measure)
Number enrolled [ Time Frame: 20 years ]
This is a contact registry. We will enroll as many patients and primary supporters/caretakers as possible.
Same as current
Complete list of historical versions of study NCT01935726 on ClinicalTrials.gov Archive Site
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Pulmonary Fibrosis Contact Registry
Pulmonary Fibrosis Contact Registry
As the name states, contact registries securely store contact information from groups of reasonably well-characterized patients (or primary supporters/caregivers) who are interested in being informed about ongoing or future research opportunities. Pulmonary fibrosis (PF) is a condition for which effective therapies have remained elusive, making drug trials and interventional research studies a mainstay in the PF arena over the last decade and for the foreseeable future. A PF Contact Registry will be a conduit to collect, analyze, and disseminate de-identified, group-level data on the clinical phenotypes of PF patients and will house contact information from patients who wish to be informed about research opportunities for which they may qualify. Data contained in the Registry will help inform research hypotheses and guide investigators as they develop research protocols by providing them with numbers of potential subjects who meet particular inclusion/exclusion criteria.

Detailed information can be found at our website at www.pulmonaryfirbrosisresearch.org.

Who will be in the Registry?

Anyone who is at least 18 years of age, can read and understand English, and either

  1. diagnosed with PF or
  2. a primary supporter or caregiver of someone living with PF

How the Registry works

Patients with PF consent to be enrolled in the Registry and may consent to be contacted by Registry personnel about opportunities for them to participate in research studies. Some of these studies (e.g., "Observing the Effects of Supplemental Oxygen on Patients with Pulmonary Fibrosis") will be conducted by Dr. Swigris and his research team—these studies will be considered Registry-affiliated. Registry participants are free to enroll in any study they wish—whether Registry-affiliated or conducted by investigators not affiliated with the Registry—i.e., non-Registry-affiliated studies. It is assumed the investigators conducting those studies will adhere to regulations governing the protection of human subjects in research. Consider a hypothetical example: an investigator in Michigan is conducting a study of the effects of oral honey on PF-related cough and would like Registry participants to consider enrollment. The investigator would petition the Registry and, if approved by the Registry Oversight Committee, Registry personnel would contact potentially eligible Registry participants to inform them of the study. The participants would then decide whether or not to contact the investigator in Michigan to be considered for enrollment. The investigatory in Michigan would be responsible for discussing the study with any potential subject, obtaining informed consent and conducting the study. All of these fall outside the purview of the Registry or its personnel.

How subjects will enroll in the Registry

Eligible participants must fill out an intake questionnaire/consent form. Contact information provided to receive a questionnaire is not stored by the Registry Data Coordinating Center (DCC) or by the study coordinator. Subjects may obtain the intake questionnaire, complete it, and submit it four different ways:

  • Complete the questionnaire/consent form and submit it online at https://dccweb.njhealth.org/sec/P3F_Swigris/Index.htm. Participants will be encouraged to print a copy for their records.
  • Enter a mailing address onto an online form at http://pulmonaryfibrosisresearch.org/contact and have a hard copy mailed to the subject. Once a signed questionnaire/consent has been sent back to the study coordinator, a copy will be made and mailed back to the participant for his/her records.
  • Fill out the form electronically at https://dccweb.njhealth.org/sec/P3F_Swigris/Index.htm and print a copy of the form, or print the form and fill it out by hand and mail or fax the completed questionnaire to the study coordinator who will then hand it off to the DCC at National Jewish Health. Participants will be encouraged to print a copy for their records.
  • Call the study coordinator toll-free at 1-855-609-0010 and have him/her mail a hard copy of the questionnaire/consent form to the subject. Once a signed questionnaire/consent has been sent back to the study coordinator, a copy will be made and mailed back to the participant for his/her records.
Observational [Patient Registry]
Time Perspective: Prospective
20 Years
Not Provided
Non-Probability Sample
Patients with pulmonary fibrosis of any cause (idiopathic, related to connective tissue disease [e.g., rheumatoid arthritis, systemic sclerosis/scleroderma, dermato-/polymyositis, sjogren's syndrome], familial or genetic) or the primary supporter/caregiver of a patient with pulmonary fibrosis
  • Pulmonary Fibrosis of Any Cause
  • Primary Supporters/Caretakers of Patients With Pulmonary Fibrosis
Not Provided
Pulmonary fibrosis patients or their caretaker/supporter
Patients with pulmonary fibrosis of any cause (idiopathic, related to connective tissue disease [e.g., rheumatoid arthritis, systemic sclerosis/scleroderma, dermato-/polymyositis, sjogren's syndrome], familial or genetic) or the primary supporter/caregiver of a patient with pulmonary fibrosis
Not Provided
 
Recruiting
50000
January 2040
January 2040   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Anyone who self-reports a diagnosis of pulmonary fibrosis and is over 18 years of age will be included in the Registry.
  • Anyone who self-reports being a primary supporter or caregiver of someone living with pulmonary fibrosis and is over the age of 18 will be included in the Registry.
  • Whoever consents to be enrolled in the Registry will presumably be able to read and write in English.

Exclusion Criteria:

  • Failure to meet inclusion criteria
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Yes
Contact: Amanda Belkin, MPH 855-609-0010 support@PFresearch.org
United States
 
 
NCT01935726
PCORI 4134
Yes
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Jeff Swigris, National Jewish Health
National Jewish Health
  • Pulmonary Fibrosis Foundation
  • Patient-Centered Outcomes Research Institute
Principal Investigator: Jeff Swigris, DO, MS National Jewish Health
National Jewish Health
August 2013