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Evaluating the Acceptability, Feasibility and Usability of Various Conversational Data Collection Software

RecruitingNAAges 18 Years - anyAllAugMend Health Inc.
NCT07336537 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This research study is being conducted to evaluate digital software tools that collect health information through conversations. The study will test how acceptable, feasible, and usable these conversational software programs are for patients with chronic pain. Purpose of the Study: The goal is to understand whether digital conversational tools can effectively gather biopsychosocial information (biological, psychological, and social factors related to health) from patients experiencing chronic pain. Biopsychosocial information includes details about your physical symptoms, emotional well-being, social circumstances, and how these factors interact to affect your health. These digital tools are designed to have conversation-like interactions with patients to collect this comprehensive health data in a more natural and engaging way. What Participation Involves: If you join this study, yo

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📋 Eligibility rules (as published)
Inclusion Criteria: * Adults aged 18 years or older * Diagnosis of chronic pain (pain lasting 3 months or longer) * Able to read and understand English * Able to provide informed consent * Willing and able to complete study procedures either at home or at the MIT.nano Immersion Lab * Access to necessary technology for home-based participation (if assigned to home-based group), or ability to travel to the MIT.nano Immersion Lab (if assigned to laboratory-based group) * Cognitively able to interact with digital data collection software and provide feedback Exclusion Criteria: * Under 18 years of age * Unable to provide informed consent * Non-English speaking * Acute pain only (pain lasting less than 3 months) * Cognitive impairment that would prevent meaningful interaction with data collection software or ability to provide valid feedback * Unable or unwilling to complete study procedures in assigned setting (home or laboratory) * Any condition that, in the opinion of the investigator, would make participation unsafe or interfere with the participant's ability to complete study procedures
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What it tests

  • Digital Biopsychosocial Conversational Data Collection Software
  • Standard Digital Questionnaire Data Collection
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Where

1 site
AugMend Health at MIT.nano Immersion Lab
Cambridge, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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