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NCT Number: NCT03494075

MyPaTH Story Booth

The MyPaTH Story Booth will use an (audio) "document" approach to elicit in depth experiential knowledge or perspectives from patients and caregivers by recording their personal stories.

Recruiting

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Pittsburgh

Pittsburgh, Pennsylvania, 15213, United States

Location status: Recruiting

Location contact

Emily L Klawson, MS

CONTACT

[email protected]

412-586-9796

Kathleen M McTigue, MD, MS, MPH

PRINCIPAL_INVESTIGATOR

About this study

Modeled after the Storycorps project and healthtalk.org, MyPaTH Story Booth will use an (audio) "document" approach to elicit in depth experiential knowledge or perspectives from patients and caregivers by recording their personal stories. Narratives provide a powerful framework for understanding patient problems and the larger process of illness, coping, and seeking health care. Narratives can provide meaning, context, and perspective for patients' situations and insight into failures in health care delivery, particularly for marginalized patients. MyPaTH Story Booth will provide simple instructions for how participants can work with an interview partner (e.g., a family member or friend) to record their story. MyPath Story Booth may be launched sequentially at each PaTH site to establish an initial archive of patient and caregiver narratives. Individuals who record narratives will be asked to provide limited "tags" to populate a searchable database (e.g., their age, sex, interview topic). The audio booth and procedures will also be made available to PaTH affiliated researchers who wish to augment the narrative database with narratives of patient partners from specific study populations.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over the age of 18

Exclusion criteria

  • Researchers will exclude individuals who are not 18 years of age or older and/or do not provide informed consent

Treatment and study plan

Primary outcomes

  1. Number of stories collected

    Time frame: September 2018

    The goal of the project is to generate a searchable archive of patient and caregiver narratives

Secondary outcomes

  1. Comparison of approaches to categorize story contents

    Time frame: Cross-sectional analysis of the first 100 stories, September 2018

    Researchers will compare how story contents are categorized using (a) qualitative research coding with survey data collected from (b) participants and (c) study staff

  2. Number of researchers who access the online story archive

    Time frame: Annually at 2 and 3 years of follow-up the number of researchers who accessed stories will be reviewed.

    To support health researchers' use of patient and caregiver narratives in formulating research questions

  3. Number of research teams who engage stakeholders through the project

    Time frame: Annually at 2 and 3 years of follow-up

    The project aims to facilitate connections between individuals who have real-world insights and experience with health care or health care delivery and health researchers.

Study contacts

Contact information is provided by the study sponsor or research team.

Emily L Klawsson, MS

CONTACT

[email protected]

412-586-9796

Kathleen M McTigue, MD

CONTACT

[email protected]

4126922940

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Registry information

Important dates

Study start
2016
Primary completion
2030
Study completion
2030
First posted
Apr 11, 2018
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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