Conversational Data Collection for Chronic Pain
(CADS Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine if digital tools can effectively collect health information about chronic pain through conversation-like interactions. Participants will use these tools, including the Digital Biopsychosocial Conversational Data Collection Software, to share details about their pain experiences, emotional well-being, and social factors. The main goal is to assess whether these tools are easy and practical for patients to use in real-world settings. Ideal participants are those who have experienced chronic pain for at least three months and can interact with digital platforms in English. As an unphased trial, this study offers a unique opportunity to contribute to innovative research that could enhance chronic pain management for many.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It seems focused on using digital tools to collect information about your chronic pain, so it's unlikely that you would need to change your medication routine.
What prior data suggests that these digital conversational tools are safe for collecting health information from patients with chronic pain?
A previous study found that patients with chronic pain responded well to using digital tools for health information collection. Research shows these tools are generally safe, as they are software-based and involve minimal risk. Unlike medications or medical devices, this software interacts with users like a conversation with a healthcare provider.
Initial findings suggest that patients have had positive experiences using these digital tools for managing chronic pain. Reports indicate that these tools are easy to use and have no known negative effects. Since this is software and not a medication, the focus is on ease and practicality for patients rather than side effects.
Overall, evidence shows the digital software is safe, user-friendly, and can be a helpful addition to managing chronic pain.12345Why are researchers excited about this trial?
Researchers are excited about the trial for the digital biopsychosocial conversational data collection software because it offers a fresh approach to understanding and managing chronic pain. Unlike traditional methods, which often rely on standard questionnaires and interviews, this digital tool allows for a more dynamic and comprehensive collection of data about patients' pain experiences, emotional well-being, and social circumstances. The software's interactive nature not only aims to improve the accuracy and depth of information gathered but also enhances patient engagement by making the process more intuitive and user-friendly. By evaluating its acceptability, feasibility, and usability, researchers hope to find out if this digital approach could lead to better insights and potentially more personalized pain management strategies.
What evidence suggests that this trial's digital data collection methods could be effective for chronic pain?
Research has shown that digital health tools, like chat software, can help manage chronic pain by gathering important health information. In this trial, participants in one arm will use the Digital Biopsychosocial Conversational Data Collection Software. This software is designed to mimic conversations with healthcare providers, making data collection more natural and engaging. One study found that these tools effectively collect data on physical symptoms, emotions, and social interactions, which are key to understanding chronic pain. Patients have reported that these digital tools are easy to use and helpful in providing a complete picture of their health. Meanwhile, participants in the control arm will use the Standard Digital Questionnaire Data Collection method. Overall, evidence suggests these digital tools offer a practical way to gather detailed health information from people with chronic pain.12567
Who Is on the Research Team?
Alexandra Therond, MA
Principal Investigator
AugMend Health
Mark Ruchman, MD
Principal Investigator
AugMend Health
Are You a Good Fit for This Trial?
This study is for adults over 18 with chronic pain lasting more than 3 months, who can read English and give informed consent. Participants should be able to complete tasks at home or travel to the MIT.nano Immersion Lab if needed, have access to technology for home participation, and be cognitively capable of interacting with digital tools.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Data Collection
Participants interact with digital software to provide biopsychosocial information about their chronic pain condition.
Follow-up
Participants are monitored for usability, feasibility, and acceptability of the digital tools.
What Are the Treatments Tested in This Trial?
Interventions
- Digital Biopsychosocial Conversational Data Collection Software
- Standard Digital Questionnaire Data Collection
Trial Overview
The trial is testing conversational software that collects health information from patients by simulating a natural conversation. It aims to see how well these tools gather comprehensive biopsychosocial data in those experiencing chronic pain.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Participants in this arm will use digital software to provide biopsychosocial information about their chronic pain condition. The software will collect data about participants' pain experiences, physical functioning, emotional well-being, social circumstances, and other health-related factors. Participants may complete study procedures at home or at the MIT.nano Immersion Lab depending on the technical requirements and study protocol. They will interact with the digital platform to provide comprehensive health information and will be asked to provide feedback on their experience with the data collection method. This arm evaluates the acceptability (whether patients find the tool appropriate and are willing to use it), feasibility (whether it can be practically implemented in real-world settings), and usability (how easy and intuitive the tool is for patients) of the digital data collection approach.
Participants in this arm will use a standard method to provide biopsychosocial information about their chronic pain condition. They will provide data about their pain experiences, physical functioning, emotional well-being, social circumstances, and other health-related factors using conventional data collection approaches. Participants may complete study procedures at home or at designated study locations depending on the study protocol. They will provide comprehensive health information through the assigned data collection method and will be asked to provide feedback on their experience. This arm serves as a comparison group to evaluate the acceptability (whether patients find the method appropriate and are willing to use it), feasibility (whether it can be practically implemented in real-world settings), and usability (how easy and intuitive the method is for patients) of standard data collection approaches.
Find a Clinic Near You
Who Is Running the Clinical Trial?
AugMend Health Inc.
Lead Sponsor
Citations
Evaluating the Acceptability, Feasibility and Usability of ...
This research study is being conducted to evaluate digital software tools that collect health information through conversations.
Effectiveness of Digital Health Interventions (DHI) in Chronic ...
The following study identifies and assesses DHIs' efficacy in specific chronic pain conditions and then extrapolates improved outcomes and ...
Conversational Data Collection for Chronic Pain (CADS Trial)
The study will test how acceptable, feasible, and usable these conversational software programs are for patients with chronic pain.
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journals.lww.com
journals.lww.com/jehp/fulltext/2025/11280/implementation_outcomes_of_a_biopsychosocial_model.493.aspxImplementation outcomes of a biopsychosocial model pain...
A prospective interventional study was conducted to evaluate the efficacy and implementation outcomes of the biopsychosocial model (BPS)-based CPM protocol ...
Patients' Experiences of Digital Health Interventions for the ...
Research regarding the effectiveness of digital health interventions (DHIs) for people living with chronic pain is widely documented, ...
Conversational Agents to Support Pain Management
This scoping review aims to comprehensively evaluate the applications and effectiveness of conversational agents in supporting pain management in adults.
Professional-Facing Digital Health Technology for the Care ...
This scoping review aims to identify the available professional-facing DHTs for chronic pain management.
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