Perceived Barriers to Patient Adherence After Pediatric Solid Organ Transplantation

NCT ID: NCT01370746

Last Updated: 2017-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

502 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-04-30

Study Completion Date

2014-04-30

Brief Summary

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In this study, doctors will observe how and when pediatric patients who have received a solid organ transplant take their prescribed medication, and determining if there are reasons that keep these patients from taking all of their medicine.

Detailed Description

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Adhering to treatment regimens after solid organ transplantation is critical for the prevention of complications, including acute and chronic organ rejection. It is important to recognize the perceived barriers to following treatment regimens and identify ways to address these barriers early in the course of treatment.

Conditions

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Organ Transplantation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cross-Sectional Study Group

Cross-sectional comparison of perceived barriers to adherence to post-transplant immunosuppressant regimens in parents/legal guardians of children 0-11 years versus adolescents 12-21 years

No interventions assigned to this group

Longitudinal Study Group

Subset of Cross-Sectional Study Group to evaluate whether perceived barriers to adherence increase with time during the first year following transplantation

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Subject and/or guardian must be able to understand and provide informed consent/assent in English or Spanish
* Male or female primary solid organ transplant patients 0-21 years of age
* Recipients at least 1 month post-transplant hospital discharge

Exclusion Criteria

* Inability or unwillingness of a participant or parent/guardian to give informed consent or comply with study protocol
* Condition or characteristic which in the opinion of the investigator makes the participant unlikely to complete the questionnaires
* Re-transplant recipient
* Multi-organ transplant recipient
Maximum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Clinical Trials in Organ Transplantation in Children

OTHER

Sponsor Role collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stuart Sweet, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Washington University School of Medicine

Lara Danziger-Isakov, MD, MPH

Role: STUDY_CHAIR

Children's Hospital Medical Center, Cincinnati

Locations

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University of Alabama

Birmingham, Alabama, United States

Site Status

Ronald Reagan UCLA Medical Center (Mattel Childrens')

Los Angeles, California, United States

Site Status

University of California San Francisco Children's Hospital

San Francisco, California, United States

Site Status

Lucile Packard Children's Hospital at Stanford

Stanford, California, United States

Site Status

University of Florida Health Sciences Center

Gainesville, Florida, United States

Site Status

Emory Children's Center

Atlanta, Georgia, United States

Site Status

Children's Hospital of Boston

Boston, Massachusetts, United States

Site Status

Washington University School of Medicine

St Louis, Missouri, United States

Site Status

Children's Hospital of New York

New York, New York, United States

Site Status

The Cleveland Clinic

Cleveland, Ohio, United States

Site Status

Nationwide Children's Hospital

Columbus, Ohio, United States

Site Status

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

Site Status

University of Pittsburgh School of Medicine

Pittsburgh, Pennsylvania, United States

Site Status

Baylor College of Medicine/Texas Children's Hospital

Houston, Texas, United States

Site Status

Children's Hospital and Regional Medical Center

Seattle, Washington, United States

Site Status

Countries

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United States

References

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Shemesh E. Barriers to adherence - To screen or not to screen, that is the question. Pediatr Transplant. 2016 Mar;20(2):188-90. doi: 10.1111/petr.12671. Epub 2016 Jan 22. No abstract available.

Reference Type BACKGROUND
PMID: 26799519 (View on PubMed)

Danziger-Isakov L, Frazier TW, Worley S, Williams N, Shellmer D, Dharnidharka VR, Gupta NA, Ikle D, Sweet SC; CTOTC-05 Consortium. Perceived barriers to medication adherence in pediatric and adolescent solid organ transplantation. Pediatr Transplant. 2016 Mar;20(2):307-15. doi: 10.1111/petr.12648. Epub 2015 Dec 16.

Reference Type RESULT
PMID: 26670870 (View on PubMed)

Related Links

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https://www.niaid.nih.gov/

National Institute of Allergy and Infectious Diseases (NIAID)

https://www.niaid.nih.gov/about/dait

Division of Allergy, Immunology, and Transplantation (DAIT)

https://www.ctotc.org/

Clinical Trials in Organ Transplantation in Children (CTOT-C)

Other Identifiers

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DAIT CTOTC-05

Identifier Type: -

Identifier Source: org_study_id

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