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Formative Usability Study

ATTR Drug Delivery Formative Usability Study

Evaluating Autoinjectors for Safe and Effective Drug Delivery

Participate in our study to help develop safer and easier-to-use medical devices for patients with ATTR and those new to injections.

Study Objectives

Why Your Participation Matters

Your input is crucial in developing safer and more effective drug delivery devices.

Identify User Interface Concerns

Help us pinpoint areas of confusion or concern in autoinjector design.

Evaluate Workflow Safety

Assess whether users can safely and effectively perform injection tasks.

Uncover Potential Use Errors

Help us identify and mitigate potential errors to enhance device safety.

Capture User Preferences

Provide valuable feedback on ease-of-use and overall device preference.

Study Information

Study Overview

Key information about the ATTR Drug Delivery Formative Usability Study

Duration

90 minutes

Virtual session from your home

Procedures

Simulate use of 4 autoinjectors on a skin pad, answer questions about your experience.

No medication administered to participants.

Sponsor & Conductor

Sponsor: ABC Corp

Conducted by: ClariMed

The Process

Your Participation Journey

What to expect when joining this formative usability study

1

Online Screening

Complete our confidential online questionnaire to determine your eligibility for the study.

2

Virtual Study Session

Participate in a 90-minute virtual session from your home, simulating autoinjector use on a provided pad.

3

Make an Impact

Your valuable feedback will directly contribute to the development of safer and more user-friendly medical devices.

Eligibility & Benefits

Who Can Participate & What You Gain

Learn about the criteria for participation and the advantages of joining our study

Eligibility Criteria

  • Lives in the United States
  • Able to read and comprehend written and spoken English
  • Twenty (20) years of age or older
  • Not currently pregnant or expecting to be pregnant soon
  • Does not, nor does an immediate family member, work in the pharmaceutical or medical device industry or for a Governmental Regulatory agency such as the FDA
  • Does not have any medical training beyond First Aid and/or CPR (with specific exceptions)
  • No severe functional impairments that prevent study participation (e.g., severe uncorrected vision/hearing issues, severe cognitive limitations)
  • Willing to be video and audio recorded
  • Meets specific criteria for either ATTR patient/surrogate or injection-naïve/caregiver user groups.

Benefits of Participation

  • Contribute to the development of safer and more effective drug delivery devices.
  • Help improve medical devices for patients with mobility/dexterity issues and those new to injections.
  • Receive compensation for your time and participation.
  • Participate from the comfort of your own home.

Frequently Asked Questions

Common questions about the ATTR Drug Delivery Formative Usability Study

Join the ATTR Drug Delivery Formative Usability Study Today

Your participation is vital in shaping the future of drug delivery devices. Take the first step by completing our screening questionnaire.

Begin Screening Now