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Clinical Trials/NCT04827381
NCT04827381
Completed
N/A

Improving Patient and Caregiver Engagement Through the Application of Data Science Methods to Audio Recorded Clinic Visits Stored in Personal Health Libraries

Dartmouth-Hitchcock Medical Center1 site in 1 country45 target enrollmentApril 15, 2021
ConditionsMultimorbidity

Overview

Phase
N/A
Intervention
Not specified
Conditions
Multimorbidity
Sponsor
Dartmouth-Hitchcock Medical Center
Enrollment
45
Locations
1
Primary Endpoint
Participant retention (Feasibility)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

In this project, the investigators will conduct a three-arm patient-randomized pilot trial in older adults with multimorbidity in ambulatory care settings to determine the feasibility, usability, and acceptability of an audio-based PHL developed with older adults and caregivers, HealthPAL.

Detailed Description

Providing digital recordings of clinical visits to patients has emerged as a new strategy to promote patient and family engagement in care. With advances in natural language processing, an opportunity exists to maximize the value of visit recordings for patients by automatically annotate key visit information (e.g., medications, tests \& imaging) with linkages to trustworthy online resources. These resources can be curated in an audio-based personal health library (PHL). In this project, the investigators will conduct a three-arm patient-randomized pilot trial in older adults with multimorbidity in ambulatory care settings to determine the feasibility, usability, and acceptability of an audio-based PHL developed with older adults and caregivers, HealthPAL. Participants in the intervention arms will receive access to an audio-based PHL with either 1) a clinic visit recording where key information is annotated and hyperlinks to trustworthy health information are provided (HealthPAL), 2) a clinic visit recording without annotations or hyperlinks, or 3) the third group of participants will receive usual care (control) with no recordings. Usability metrics and satisfaction will be assessed at two weeks. Preliminary data on the impact of HealthPAL on patient ability to seek, find and use health information with high confidence and patient activation, as well caregiver preparedness will also be gathered.

Registry
clinicaltrials.gov
Start Date
April 15, 2021
End Date
February 4, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paul J. Barr

Associate Professor, The Dartmouth Institute for Health Policy & Clinical Practice Geisel School of Medicine at Dartmouth

Dartmouth-Hitchcock Medical Center

Eligibility Criteria

Inclusion Criteria

  • (1) ≥ 65 years
  • (2) with multimorbidity
  • (3) plan on receiving ongoing care at the clinic for the subsequent month
  • (4) access to internet.
  • The investigators will only include patients of clinicians (MDs, NPs) who (1) are based at the study clinic; (2) who treat adult patients.

Exclusion Criteria

  • (1) who have a six-item screener (SIS) of cognitive function score ≤ 4 and/or for those with a defined caregiver, whose proxy has not provided consent for the patient's participation
  • (2) with schizophrenia, or other psychotic disorders, substance-abuse disorders, and with uncorrectable vision or hearing impairment
  • (3) who reside in nursing homes, long-term care, skilled nursing, or hospice.
  • The investigators will exclude clinicians who (1) are trainees, e.g., medical students or residents; or (2) commonly audio or video record clinic visits for patient's personal use.

Outcomes

Primary Outcomes

Participant retention (Feasibility)

Time Frame: Two weeks from baseline

The proportion of included participants completing the two-week (T1) follow up assessment.

Listening rates (Acceptability)

Time Frame: Two weeks from baseline

The proportion of patients who listen to their recordings.

System Usability Scale (SUS)

Time Frame: Two weeks from baseline

10-item PROM. A score ≥68 points (0-100) indicates above average usability

Acceptability of Intervention Measure (AIM)

Time Frame: Two weeks from baseline

Four-item PROM assessing acceptability of intervention. Higher score indicates higher acceptability of the intervention.

Intervention Appropriateness Measure (IAM)

Time Frame: Two weeks from baseline

Four-item PROM assessing feasibility of intervention. Higher score indicates greater appropriateness of the intervention.

Feasibility of Intervention Measure (FIM)

Time Frame: Two weeks from baseline

Four-item PROM assessing feasibility of intervention. Higher score indicates higher feasibility of the intervention.

Study Sites (1)

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