Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT05441306

Personal Health Libraries for Formerly Incarcerated Individuals

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Yale University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a randomized pilot study to test the acceptance and use of PerHL among formerly incarcerated individuals

Detailed description

Eligible participants will be enrolled after providing informed consent .Participants will then complete a baseline assessment. After the interview, eligible participants will be randomly assigned to the intervention or control group. The research assistant (RA) will be blinded to the randomization allocation until after the consent process. For the purposes of this study, permuted block randomization with random block sizes of 2, 4 and 6 will be used. Intervention: Those randomized to the intervention arm will have access to PerHL. The intervention group will watch a demonstration by the RA and will practice using PerHL for 10-15 minutes, i.e. taking a picture of a document and uploading to PerHL, entering specific information, voice recording an appointment reminder. The RA will be responsible for providing technical support and assist with the need for initial support, e.g. phone-call or text-based support. At baseline, participants will be asked to provide a list of every organization they visited that may have health and health-related social information on them and receive consent to request their information to be sent to the participant and the study team on their behalf. Control: Participants randomized to the control arm will receive the standard of care patient portal (Epic®MyChart). The RA will give them an informational pamphlet outlining key features of the patient portal and guide them through the steps for signing up for a MyChart account, assist them to sign up, add the standard patient portal MyChart app to their phone, and provide them with the MyChart technical support hotline. Study Procedures: During the intervention phase, all participants will meet with the RA at baseline, 1- and 3 months. During the study, each participant will be asked to provide at least 5 verified locators who are likely to have knowledge of their whereabouts throughout follow-up. Each participant will be provided with $50 payment to participants for each completion of surveys at baseline, 1, 3 months. In addition, participants will be given $10 each month to travel to a location with free wireless so their information can be uploaded to the cloud and a list of available locations. In total, each participant will receive $180 for participation. For the 1- and 3-month follow-up period, the RA will ask participants to bring information collected and uploaded in PerHL and additional information that is important to the participant but was not uploaded.

Conditions

Interventions

TypeNameDescription
DEVICEPersonal Health Library (PerHL) + MyChartParticipants randomized to the PerHL arm will have access to PerHL + the standard of care patient portal (Epic®MyChart).
DEVICEEpic®MyChartParticipants randomized to the control arm will receive the standard of care patient portal (Epic®MyChart).

Timeline

Start date
2025-12-01
Primary completion
2026-02-01
Completion
2026-02-28
First posted
2022-07-01
Last updated
2025-09-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05441306. Inclusion in this directory is not an endorsement.