COVID-19
Conditions
Brief summary
The long-term objective of SCALE-UP II is to increase the reach, uptake, and sustainability of COVID-19 testing among underserved populations. Through RADx-UP Phase I funding (SCALE-UP Utah), the team has established population health management (PHM) interventions that have been used since Feb 2021 to increase the uptake of COVID-19 testing and vaccination among community health center patients. Interventions are based on a PHM approach that uses widely available technology (i.e. cell phones and text messaging). SCALE-UP II will both build on SCALE-UP Utah PHM interventions and investigate novel resource conservation approaches (i.e., Request-Patient Navigation vs. No Patient Navigation and text messaging vs. conversational agent). SCALE-UP II builds on long standing partnerships among the University of Utah Clinical and Translational Science Institute (UofU CTSI), Association for Utah Community Health (AUCH), CHCs, and the Utah Department of Health(UDOH). CTSI and SCALE-UP II investigators are leading several COVID-19 initiatives that drive public health response and state government policies in Utah. Thus, the UofU team is uniquely positioned to lead this project.
Detailed description
Racial/ethnic minority, low socioeconomic status (SES), and rural populations suffer profound health inequities across a wide variety of diseases and conditions, including COVID-19. For example, as of June 2021, the cumulative COVID case rate in Utah per 100,000 was 10,803 among Whites vs. 17,541 among Latinos. The positivity rate was 14% among Whites vs. 24% among Latinos. Similar disparities persist across the nation for vaccination rates between urban vs. rural, high vs. low SES, and White vs. non-White populations. Low vaccination rates leave underserved populations at risk for local outbreaks, and more contagious and severe variants. Thus, interventions targeting these populations at the interplay between testing and vaccination among underserved populations are critical for pandemic control. Not only do underserved populations experience profound health inequities, but there is also a critical digital divide between high and low resource healthcare systems. Low resource settings are far less likely to adopt Health Information Technology approaches, and often do not have the capacity to implement large scale population health management (PHM) efforts utilizing data analytics and automated patient outreach. As such, research is needed utilizing targeted PHM approaches that proactively identify, reach, and navigate vulnerable patients to both increase opportunities to engage in vaccination and testing, and to address barriers to engagement. Community Health Centers (CHCs) are optimal settings for implementation of PHM interventions to increase the uptake of COVID-19 testing and vaccination among underserved populations. Eleven Utah CHC systems are participating in SCALE-UP II. Their 38 primary care clinics serve over 112,000 unique patients annually (36% Latino, 10% Native American, 63% \<100% poverty level, 57% uninsured, and 42% of clinics are in rural/frontier areas). SCALE UP II is comprised of two distinct studies, the Text Message (TM) study and the Conversational Agent (CA) study. Patients will be triaged into one of two studies based on self-reported ownership of a smart phone with internet access. Patients who report not owning a smart phone with internet access will be included in the TM study. Additionally, patients who do not respond to the question regarding smart phone ownership will be included in the TM study. Patients who self-report ownership of a smart phone with internet access will be included in the CA study. SCALE-UP II: CA study will implement and evaluate practical, accessible, and scalable PHM interventions to increase COVID-19 testing and vaccine uptake based on the best evidence available, patients' specific barriers and hesitancy factors, and extensive collaboration with CHCs, AUCH, and UDHHS. This study is a 2x2 design with patients being initially randomized between receiving either text messages or the link to a conversational agent as well as into two distinct types of available patient navigation, Request-PN or No PN. Text Messaging (TM): bidirectional text messaging to connect patients to vaccination or mailed at-home rapid test kits for use, as needed. Conversational Agent (CA): automated, scripted and interactive agent used to mimic human interaction to: 1) elicit specific hesitancy factors and barriers to testing; 2) provide tailored information to address each individual's hesitancy factors and barriers to testing; and 3) offer access to at-home rapid test kits. Patient Navigation (PN): phone call from a community health worker to help address hesitancy and barriers, and to offer at-home rapid test kits. This study will examine two distinct forms of Patient Navigation: Request PN and No PN. Each patient will be randomized to receive either Request PN or No PN. Request PN allows patients to request patient navigation by responding PERSON to a text message/conversational agent. Patients who are randomized to receive No PN will not be provided the opportunity to speak with a patient navigator. The primary outcome, Reach-Accept Testing, captures whether patients requests an at-home test kit and confirmed their mailing address. Secondary outcomes include: Testing (i.e. the proportion of participants who self-report having used an at-home test at least once during follow-up) as well as several implementation outcomes including Reach-Engage Testing (proportion of patients that reply to an offer to receive an at-home rapid test kit), PN-Request (proportion in PN who requested patient navigation), PN-Engage (proportion in PB who talked to a patient navigator), and Opt-Out. The outcomes and compared groups provided for the Smartphone study are main effects for delivery mechanism (Chatbot & TM), main effects for PN (PN & No PN), and main effects for message frequency (10-day & 30-day). SCALE-UP II will include a Consortium Data Reporting Unit (CDRU) consisting of a Data Manager and one member the project's biomedical informatics team. The unit will attend regular meetings and dissemination activities organized by the CDCC. The CDRU will seek guidance from the CDCC with regard to data acquisition and consent for data sharing. As required by the NIH, SCALE-UP II will collect RADx-UP Tier 1 Common Data Elements for study participants who receive an at-home COVID test through the project. These data will be collected through surveys administered one month after the participant receives their at-home test. Data will be standardized according to the data dictionary provided by the CDCC. Our CDRU will work closely with the CDCC to establish a protocol for frequency, format, and exchange of data. SCALE-UP II will share identifiable data with the CDCC and NIH for the Data Hub as well as future research. Participants who complete the survey data will first complete an informed consent process. The informed consent will be administered to the patient at the time of survey collection. Lighthouse Research and Development will conduct phone surveys to assess patient reported use of COVID-19 at-home testing (\ 2,300 participants) among patients who received test kits and do no respond to the online survey request. Lighthouse will send notifications (e.g., postcards, text messages, voice messages, etc.) to participants to alert them of the opportunity to complete the survey online or over the phone. Interviewers will complete up to 15 call attempts across weekday, evening, and weekend calling shifts over a one-month period to each participant. Patients will be compensated with a gift card for completing the survey.
Interventions
Participants in the TM condition will receive HIPAA-compliant bidirectional text messages. These texts will include a brief message alerting patients that they are eligible to receive a test kit and asking participants if they would like to receive a test kit. Participants who reply yes will receive an additional message with information about how to receive a test kit.
Patients in the CA condition will receive a link to an automated, scripted and interactive conversational agent used to mimic human interaction to: 1) elicit specific hesitancy factors and barriers to testing; 2) provide tailored information to address each individual's hesitancy factors and barriers to testing; and 3) offer access to at-home rapid test kits.
Participants in the PN condition will receive a call from a Community Health Worker to assist with the process of receiving a COVID test. At this time the participant has the option to opt-out of this follow up phone call. The patient navigation from the Community Health Worker includes practical advice in addressing barriers to testing such as logistics, as well as fear, skepticism, and hesitancy. There are two distinct different types of patient navigation. A person can be randomly assigned to either type, or no PN, or a combination of the two types.
Sponsors
Study design
Masking description
Patients will not know what intervention arm they are in.
Intervention model description
Patient-level, four-arm randomized design for Population Health Management interventions: (1) TM + No PN, (2) TM + Request PN, (3) CA + No PN, or (4) CA + Request PN
Eligibility
Inclusion criteria
* current patient of a participating community health center * have a working cellphone, * have phone number listed in existing electronic medical record at their participating clinic * speak English or Spanish.
Exclusion criteria
* Minors
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Reach-Accept Testing | Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message] Every 10 or 30 days from intervention messaging for 90 days dependent on group randomization. | Number of patients who requested a test kit and confirmed their mailing address. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Reach-Engage Testing | Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message] | Number of patients that reply to an offer to receive an at-home rapid test kit |
| PN-Request | Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message] | Number of participants who were assigned to PN groups who requested patient navigation. |
| PN-Engage | Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message] | Number of participants who were in PN groups who talked to a patient navigator. |
| Opt Out | Daily [up to 90 days post intervention message] | Number of participants who replied to stop receiving study interventions. Participants could opt-out at any time regardless of message timing. |
| Self-reported Testing | 90 days post intervention message | Participant self-reported testing as completed. Reported only for participants who requested COVID-19 test kits from the study and responded to follow-up messages. |
Countries
United States
Participant flow
Recruitment details
This study recruited participants in partnership with the Association for Utah Community Health and its affiliated Community Health Centers (CHCs). Three CHCs with 12 primary care clinics participated. Eligible patients had an appointment at one of the participating CHCs in the last 3 years, were 18 years and older, and had a valid cellphone number in the CHC EHR. Specific to the Conversational Agent group: these patients had also replied to a TM that they did have a Smart Phone.
Pre-assignment details
1. Opted Out- opted out after receiving introductory text but before randomization 2. Smart Phone- Participant responded that they do have a Smart Phone
Participants by arm
| Arm | Count |
|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day Patients in this group received a link to an automated scripted and interactive conversation agent used to mimic human interaction to: 1) elicit specific hesitancy factors and barriers to testing; 2) provide tailored information to address each individual's hesitancy factors and barriers to testing; and 3) offer access to at-home rapid test kits. Participants in this group did not receive Patient Navigation, and outreach frequency was intervention message delivered every 10 days for a total of 6 messages. | 261 |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day Patients in this group received a link to an automated scripted and interactive conversation agent used to mimic human interaction to: 1) elicit specific hesitancy factors and barriers to testing; 2) provide tailored information to address each individual's hesitancy factors and barriers to testing; and 3) offer access to at-home rapid test kits. Participants in this group did not receive Patient Navigation, and outreach frequency was intervention message delivered every 30 days for a total of 3 messages. | 264 |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day Patients in this group received a link to an automated scripted and interactive conversation agent used to mimic human interaction to: 1) elicit specific hesitancy factors and barriers to testing; 2) provide tailored information to address each individual's hesitancy factors and barriers to testing; and 3) offer access to at-home rapid test kits. Participants in this group could receive Patient Navigation. Patient navigation was a phone call from a community health worker that gave practical advice in addressing barriers to testing. Outreach frequency was intervention message delivered every 10 days for a total of 6 messages. | 264 |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day Patients in this group received a link to an automated scripted and interactive conversation agent used to mimic human interaction to: 1) elicit specific hesitancy factors and barriers to testing; 2) provide tailored information to address each individual's hesitancy factors and barriers to testing; and 3) offer access to at-home rapid test kits. Participants in this group could receive Patient Navigation. Patient navigation was a phone call from a community health worker that gave practical advice in addressing barriers to testing. Outreach frequency was intervention message delivered every 30 days for a total of 3 messages. | 262 |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day Patients in this group received a bidirectional text message that included a brief message alerting patients they were eligible to receive a test kit. Participants in this group did not receive Patient Navigation, and outreach frequency was intervention message delivered every 10 days for a total of 6 messages. | 265 |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day Patients in this group received a bidirectional text message that included a brief message alerting patients they were eligible to receive a test kit. Participants in this group did not receive Patient Navigation, and outreach frequency was intervention message delivered every 30 days for a total of 3 messages. | 265 |
| Text Message (TM) + Patient Navigation (PN) + 10 Day Patients in this group received a bidirectional text message that included a brief message alerting patients they were eligible to receive a test kit. Participants in this group could receive Patient Navigation. Patient navigation was a phone call from a community health worker that gave practical advice in addressing barriers to testing. Outreach frequency was intervention message delivered every 10 days for a total of 6 messages. | 270 |
| Text Message (TM) + Patient Navigation (PN) + 30 Day Patients in this group received a bidirectional text message that included a brief message alerting patients they were eligible to receive a test kit. Participants in this group could receive Patient Navigation. Patient navigation was a phone call from a community health worker that gave practical advice in addressing barriers to testing. Outreach frequency was intervention message delivered every 30 days for a total of 3 messages. | 266 |
| Total | 2,117 |
Baseline characteristics
| Characteristic | Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | Text Message (TM) + Patient Navigation (PN) + 10 Day | Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | Text Message (TM) + Patient Navigation (PN) + 30 Day | Total |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | 48.83 Years STANDARD_DEVIATION 14.93 | 48.34 Years STANDARD_DEVIATION 14.23 | 48.89 Years STANDARD_DEVIATION 14.22 | 47.92 Years STANDARD_DEVIATION 14.4 | 49.88 Years STANDARD_DEVIATION 15.38 | 49.79 Years STANDARD_DEVIATION 15.36 | 49.38 Years STANDARD_DEVIATION 14.55 | 49.13 Years STANDARD_DEVIATION 13.85 | 49.02 Years STANDARD_DEVIATION 14.62 |
| CHC CHC 1 | 165 Participants | 162 Participants | 163 Participants | 162 Participants | 162 Participants | 166 Participants | 160 Participants | 166 Participants | 1306 Participants |
| CHC CHC 2 | 34 Participants | 33 Participants | 36 Participants | 34 Participants | 36 Participants | 36 Participants | 35 Participants | 34 Participants | 278 Participants |
| CHC CHC 3 | 65 Participants | 67 Participants | 66 Participants | 69 Participants | 66 Participants | 68 Participants | 66 Participants | 66 Participants | 533 Participants |
| Insurance Status Private | 69 Participants | 88 Participants | 71 Participants | 85 Participants | 80 Participants | 76 Participants | 63 Participants | 78 Participants | 610 Participants |
| Insurance Status Public | 44 Participants | 45 Participants | 43 Participants | 38 Participants | 44 Participants | 40 Participants | 47 Participants | 42 Participants | 343 Participants |
| Insurance Status Uninsured | 151 Participants | 129 Participants | 151 Participants | 142 Participants | 140 Participants | 154 Participants | 151 Participants | 146 Participants | 1164 Participants |
| Language English | 127 Participants | 141 Participants | 124 Participants | 134 Participants | 128 Participants | 130 Participants | 125 Participants | 117 Participants | 1026 Participants |
| Language Other | 5 Participants | 3 Participants | 3 Participants | 4 Participants | 3 Participants | 7 Participants | 5 Participants | 5 Participants | 35 Participants |
| Language Spanish | 123 Participants | 113 Participants | 128 Participants | 121 Participants | 126 Participants | 125 Participants | 123 Participants | 134 Participants | 993 Participants |
| Language Unknown | 9 Participants | 5 Participants | 10 Participants | 6 Participants | 7 Participants | 8 Participants | 8 Participants | 10 Participants | 63 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity American Indian/Alaska Native | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 1 Participants | 3 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity Asian | 3 Participants | 0 Participants | 1 Participants | 3 Participants | 1 Participants | 1 Participants | 1 Participants | 4 Participants | 14 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity Black/African American | 1 Participants | 3 Participants | 1 Participants | 3 Participants | 3 Participants | 5 Participants | 3 Participants | 0 Participants | 19 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity Hawaiian/Pacific Islander | 1 Participants | 1 Participants | 2 Participants | 0 Participants | 1 Participants | 1 Participants | 1 Participants | 1 Participants | 8 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity Hispanic or Latino/a | 137 Participants | 139 Participants | 140 Participants | 142 Participants | 144 Participants | 144 Participants | 152 Participants | 160 Participants | 1158 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity Multi-race | 4 Participants | 5 Participants | 3 Participants | 2 Participants | 6 Participants | 4 Participants | 1 Participants | 0 Participants | 25 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity Unknown | 25 Participants | 21 Participants | 21 Participants | 22 Participants | 22 Participants | 22 Participants | 19 Participants | 19 Participants | 171 Participants |
| Race/Ethnicity, Customized Race/Ehtnicity White Non-Hispanic | 93 Participants | 92 Participants | 97 Participants | 93 Participants | 86 Participants | 93 Participants | 84 Participants | 81 Participants | 719 Participants |
| SCALE-UP I Randomization Not enrolled in SCALE UP I | 82 Participants | 80 Participants | 86 Participants | 83 Participants | 81 Participants | 86 Participants | 83 Participants | 83 Participants | 664 Participants |
| SCALE-UP I Randomization TM | 81 Participants | 79 Participants | 79 Participants | 80 Participants | 81 Participants | 81 Participants | 79 Participants | 81 Participants | 641 Participants |
| SCALE-UP I Randomization TM+PN | 101 Participants | 103 Participants | 100 Participants | 102 Participants | 102 Participants | 103 Participants | 99 Participants | 102 Participants | 812 Participants |
| Sex/Gender, Customized Sex Female | 188 Participants | 181 Participants | 182 Participants | 191 Participants | 163 Participants | 186 Participants | 179 Participants | 181 Participants | 1451 Participants |
| Sex/Gender, Customized Sex Male | 75 Participants | 81 Participants | 83 Participants | 74 Participants | 101 Participants | 84 Participants | 82 Participants | 85 Participants | 665 Participants |
| Sex/Gender, Customized Sex Unknown | 1 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants |
| Urban/Rural Rural | 33 Participants | 32 Participants | 37 Participants | 34 Participants | 34 Participants | 37 Participants | 34 Participants | 36 Participants | 277 Participants |
| Urban/Rural Urban | 231 Participants | 230 Participants | 228 Participants | 231 Participants | 230 Participants | 233 Participants | 227 Participants | 230 Participants | 1840 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk | EG004 affected / at risk | EG005 affected / at risk | EG006 affected / at risk | EG007 affected / at risk |
|---|---|---|---|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 261 | 0 / 264 | 0 / 264 | 0 / 262 | 0 / 265 | 0 / 265 | 0 / 270 | 0 / 266 |
| other Total, other adverse events | 0 / 261 | 0 / 264 | 0 / 264 | 0 / 262 | 0 / 265 | 0 / 265 | 0 / 270 | 0 / 266 |
| serious Total, serious adverse events | 0 / 261 | 0 / 264 | 0 / 264 | 0 / 262 | 0 / 265 | 0 / 265 | 0 / 270 | 0 / 266 |
Outcome results
Reach-Accept Testing
Number of patients who requested a test kit and confirmed their mailing address.
Time frame: Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message] Every 10 or 30 days from intervention messaging for 90 days dependent on group randomization.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | Reach-Accept Testing | 47 Participants |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | Reach-Accept Testing | 41 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | Reach-Accept Testing | 41 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | Reach-Accept Testing | 45 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | Reach-Accept Testing | 142 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | Reach-Accept Testing | 139 Participants |
| Text Message (TM) + Patient Navigation (PN) + 10 Day | Reach-Accept Testing | 151 Participants |
| Text Message (TM) + Patient Navigation (PN) + 30 Day | Reach-Accept Testing | 123 Participants |
Opt Out
Number of participants who replied to stop receiving study interventions. Participants could opt-out at any time regardless of message timing.
Time frame: Daily [up to 90 days post intervention message]
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | Opt Out | 14 Participants |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | Opt Out | 2 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | Opt Out | 27 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | Opt Out | 13 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | Opt Out | 23 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | Opt Out | 3 Participants |
| Text Message (TM) + Patient Navigation (PN) + 10 Day | Opt Out | 15 Participants |
| Text Message (TM) + Patient Navigation (PN) + 30 Day | Opt Out | 9 Participants |
PN-Engage
Number of participants who were in PN groups who talked to a patient navigator.
Time frame: Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message]
Population: Groups analyzed for this outcome are only PN groups/arms. No Patient Navigation (NoPN) groups were not analyzed for this outcome since patient navigation was not offered to those groups.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | PN-Engage | 0 Participants |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | PN-Engage | 0 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | PN-Engage | 2 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | PN-Engage | 2 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | PN-Engage | 0 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | PN-Engage | 0 Participants |
| Text Message (TM) + Patient Navigation (PN) + 10 Day | PN-Engage | 2 Participants |
| Text Message (TM) + Patient Navigation (PN) + 30 Day | PN-Engage | 0 Participants |
PN-Request
Number of participants who were assigned to PN groups who requested patient navigation.
Time frame: Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message]
Population: Groups analyzed for this outcome are only PN groups/arms. No Patient Navigation (NoPN) groups were not analyzed for this outcome since patient navigation was not offered to those groups.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | PN-Request | 0 Participants |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | PN-Request | 0 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | PN-Request | 3 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | PN-Request | 3 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | PN-Request | 0 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | PN-Request | 0 Participants |
| Text Message (TM) + Patient Navigation (PN) + 10 Day | PN-Request | 3 Participants |
| Text Message (TM) + Patient Navigation (PN) + 30 Day | PN-Request | 1 Participants |
Reach-Engage Testing
Number of patients that reply to an offer to receive an at-home rapid test kit
Time frame: Every 10 or 30 days dependent on group randomization [up to 90 days post intervention message]
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | Reach-Engage Testing | 90 Participants |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | Reach-Engage Testing | 73 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | Reach-Engage Testing | 78 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | Reach-Engage Testing | 68 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | Reach-Engage Testing | 155 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | Reach-Engage Testing | 154 Participants |
| Text Message (TM) + Patient Navigation (PN) + 10 Day | Reach-Engage Testing | 171 Participants |
| Text Message (TM) + Patient Navigation (PN) + 30 Day | Reach-Engage Testing | 145 Participants |
Self-reported Testing
Participant self-reported testing as completed. Reported only for participants who requested COVID-19 test kits from the study and responded to follow-up messages.
Time frame: 90 days post intervention message
Population: Reported only for participants who requested COVID-19 test kits from the study and responded to follow-up messages.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 Day | Self-reported Testing | 18 Participants |
| Conversational Agent (CA) + No Patient Navigation (PN) + 30 Day | Self-reported Testing | 16 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 10 Day | Self-reported Testing | 13 Participants |
| Conversational Agent (CA) + Patient Navigation (PN) + 30 Day | Self-reported Testing | 13 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 10 Day | Self-reported Testing | 32 Participants |
| Text Message (TM) + No Patient Navigation (NoPN) + 30 Day | Self-reported Testing | 37 Participants |
| Text Message (TM) + Patient Navigation (PN) + 10 Day | Self-reported Testing | 41 Participants |
| Text Message (TM) + Patient Navigation (PN) + 30 Day | Self-reported Testing | 25 Participants |