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Completed

NCT Number: NCT04469894

Health Insurance Literacy and Challenges in Accessing Health Services in Niemann-Pick

This study is a US based qualitative PRO research study to document the health insurance literacy as well as the patient experience in Niemann-Pick as it relates to accessing desired care, services and medications for patients.

The outcome of this research will be used to inform various other workstreams as NNPDF works to assist families.

The core research objectives are to understand the following from Niemann-Pick patients and their families in the US

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Key information

About this study

This study is a US based qualitative PRO research study to document the health insurance literacy as well as the patient experience in Niemann-Pick as it relates to accessing desired care, services and medications for patients.

The outcome of this research will be used to inform various other workstreams as NNPDF works to assist families.

The core research objectives are to understand the following from Niemann-Pick patients and their families in the US;

  • Level of health insurance literacy through assessment of health insurance terminology, and self-reported insights regarding information seeking, document literacy and cognitive skills
  • If they have healthcare insurance, and if not, why not
  • Types (including name) of insurance by which Niemann-Pick families are covered
  • Information regarding Medicaid Waivers
  • Attributes of insurance plans including, but not limited to;
  • Deductible amounts for individual and family
  • Out of pocket maximums for individual and family
  • Insurance premiums
  • Associated Health Savings Accounts
  • Associated Cost Sharing requirements
  • Services, drugs and assistive devices covered
  • What the perceived out-of-pocket costs are for Niemann-Pick families (annually)
  • When out-of-pocket maximums are perceived to be met for Niemann-Pick families
  • Patient and HCP experience in terms of challenges with accessing desired care and coverage
  • Where are families experiencing challenges with accessing desired care and coverage? (drugs, assistive devices, services) Is it different for the different phenotypes of the disease?
  • What is the challenge? (financial, time, stress, others)
  • What is the life impact of that challenge? (work and educational impact, lack or delay of treatment, others)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Participant must be a person with Niemann-Pick disease who is 18 years or older or The parent/legal guardian of a person with Niemann-Pick disease. Please note: Parents whose child has passed on are able to participate in the RSVP. Parents whose child has passed on in the last two years are also able to participate in the interview. Please note that only one family member will be eligible to complete the RSVP and interview for one family.
  • Confirmed diagnosis of Niemann-Pick disease, confirmed by membership in the NNPDF or by provision of a proof of disease form
  • Able to read, write and communicate in English
  • Able to grant informed consent
  • Willing to complete a survey and RSVP, and to participate in a 30-minute telephone interview
  • Ability to view or receive a document from the interviewer before or during the interview (web browser, ability to receive a text, fax or document by mail)

Exclusion criteria

  • Inability to meet any of the above 6 criteria

Treatment and study plan

Primary outcomes

  1. Health Insurance Literacy

    Time frame: July 2020- September

    Health insurance literacy will be measured by a score on a brief quiz regarding health insurance key terms as well as self-ratings regarding various aspects of the participants' ability to navigate and understand insurance

  2. Health Insurance Coverage

    Time frame: July 2020- September

    Health insurance coverage will be measured by the different multiple choice and open-ended questions based on the services available under the participants' insurance plan as well as their reported difficulty with navigating their plan and obtaining what they need for Niemann-Pick

Sponsors and collaborators

Lead sponsor

National Niemann-Pick Disease Foundation

Other

Collaborators

  • Engage Health Inc.
  • Icahn School of Medicine at Mount Sinai

Registry information

Official study title

Understanding Health Insurance Literacy and Challenges in Accessing Health Services in Niemann-Pick Disease Through the Eyes of Patients and Families

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jul 14, 2020
Registry last updated
Oct 6, 2020

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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