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SCALE-UP Utah II: Community-Academic Partnership to Address COVID-19 Conversational Agent Study

SCALE-UP Utah II: Community-Academic Partnership to Address COVID-19 Testing and Vaccination Among Utah Community Health Centers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05533359
Enrollment
2117
Registered
2022-09-09
Start date
2023-01-15
Completion date
2023-11-30
Last updated
2025-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19

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

Utah Department of Health
CollaboratorOTHER
Association for Utah Community Health
CollaboratorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
National Institute on Minority Health and Health Disparities (NIMHD)
CollaboratorNIH
University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)

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

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Reach-Accept TestingEvery 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

MeasureTime frameDescription
Reach-Engage TestingEvery 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-RequestEvery 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-EngageEvery 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 OutDaily [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 Testing90 days post intervention messageParticipant 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

ArmCount
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
Total2,117

Baseline characteristics

CharacteristicConversational Agent (CA) + Patient Navigation (PN) + 10 DayConversational Agent (CA) + Patient Navigation (PN) + 30 DayText Message (TM) + No Patient Navigation (NoPN) + 10 DayText Message (TM) + No Patient Navigation (NoPN) + 30 DayConversational Agent (CA) + No Patient Navigation (PN) + 30 DayText Message (TM) + Patient Navigation (PN) + 10 DayConversational Agent (CA) + No Patient Navigation (NoPN) + 10 DayText Message (TM) + Patient Navigation (PN) + 30 DayTotal
Age, Continuous48.83 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 Participants162 Participants163 Participants162 Participants162 Participants166 Participants160 Participants166 Participants1306 Participants
CHC
CHC 2
34 Participants33 Participants36 Participants34 Participants36 Participants36 Participants35 Participants34 Participants278 Participants
CHC
CHC 3
65 Participants67 Participants66 Participants69 Participants66 Participants68 Participants66 Participants66 Participants533 Participants
Insurance Status
Private
69 Participants88 Participants71 Participants85 Participants80 Participants76 Participants63 Participants78 Participants610 Participants
Insurance Status
Public
44 Participants45 Participants43 Participants38 Participants44 Participants40 Participants47 Participants42 Participants343 Participants
Insurance Status
Uninsured
151 Participants129 Participants151 Participants142 Participants140 Participants154 Participants151 Participants146 Participants1164 Participants
Language
English
127 Participants141 Participants124 Participants134 Participants128 Participants130 Participants125 Participants117 Participants1026 Participants
Language
Other
5 Participants3 Participants3 Participants4 Participants3 Participants7 Participants5 Participants5 Participants35 Participants
Language
Spanish
123 Participants113 Participants128 Participants121 Participants126 Participants125 Participants123 Participants134 Participants993 Participants
Language
Unknown
9 Participants5 Participants10 Participants6 Participants7 Participants8 Participants8 Participants10 Participants63 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
American Indian/Alaska Native
0 Participants1 Participants0 Participants0 Participants1 Participants0 Participants0 Participants1 Participants3 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
Asian
3 Participants0 Participants1 Participants3 Participants1 Participants1 Participants1 Participants4 Participants14 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
Black/African American
1 Participants3 Participants1 Participants3 Participants3 Participants5 Participants3 Participants0 Participants19 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
Hawaiian/Pacific Islander
1 Participants1 Participants2 Participants0 Participants1 Participants1 Participants1 Participants1 Participants8 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
Hispanic or Latino/a
137 Participants139 Participants140 Participants142 Participants144 Participants144 Participants152 Participants160 Participants1158 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
Multi-race
4 Participants5 Participants3 Participants2 Participants6 Participants4 Participants1 Participants0 Participants25 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
Unknown
25 Participants21 Participants21 Participants22 Participants22 Participants22 Participants19 Participants19 Participants171 Participants
Race/Ethnicity, Customized
Race/Ehtnicity
White Non-Hispanic
93 Participants92 Participants97 Participants93 Participants86 Participants93 Participants84 Participants81 Participants719 Participants
SCALE-UP I Randomization
Not enrolled in SCALE UP I
82 Participants80 Participants86 Participants83 Participants81 Participants86 Participants83 Participants83 Participants664 Participants
SCALE-UP I Randomization
TM
81 Participants79 Participants79 Participants80 Participants81 Participants81 Participants79 Participants81 Participants641 Participants
SCALE-UP I Randomization
TM+PN
101 Participants103 Participants100 Participants102 Participants102 Participants103 Participants99 Participants102 Participants812 Participants
Sex/Gender, Customized
Sex
Female
188 Participants181 Participants182 Participants191 Participants163 Participants186 Participants179 Participants181 Participants1451 Participants
Sex/Gender, Customized
Sex
Male
75 Participants81 Participants83 Participants74 Participants101 Participants84 Participants82 Participants85 Participants665 Participants
Sex/Gender, Customized
Sex
Unknown
1 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants1 Participants
Urban/Rural
Rural
33 Participants32 Participants37 Participants34 Participants34 Participants37 Participants34 Participants36 Participants277 Participants
Urban/Rural
Urban
231 Participants230 Participants228 Participants231 Participants230 Participants233 Participants227 Participants230 Participants1840 Participants

Adverse events

Event typeEG000
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 / 2610 / 2640 / 2640 / 2620 / 2650 / 2650 / 2700 / 266
other
Total, other adverse events
0 / 2610 / 2640 / 2640 / 2620 / 2650 / 2650 / 2700 / 266
serious
Total, serious adverse events
0 / 2610 / 2640 / 2640 / 2620 / 2650 / 2650 / 2700 / 266

Outcome results

Primary

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.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 DayReach-Accept Testing47 Participants
Conversational Agent (CA) + No Patient Navigation (PN) + 30 DayReach-Accept Testing41 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 10 DayReach-Accept Testing41 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 30 DayReach-Accept Testing45 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 10 DayReach-Accept Testing142 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 30 DayReach-Accept Testing139 Participants
Text Message (TM) + Patient Navigation (PN) + 10 DayReach-Accept Testing151 Participants
Text Message (TM) + Patient Navigation (PN) + 30 DayReach-Accept Testing123 Participants
Secondary

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]

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 DayOpt Out14 Participants
Conversational Agent (CA) + No Patient Navigation (PN) + 30 DayOpt Out2 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 10 DayOpt Out27 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 30 DayOpt Out13 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 10 DayOpt Out23 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 30 DayOpt Out3 Participants
Text Message (TM) + Patient Navigation (PN) + 10 DayOpt Out15 Participants
Text Message (TM) + Patient Navigation (PN) + 30 DayOpt Out9 Participants
Secondary

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.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 DayPN-Engage0 Participants
Conversational Agent (CA) + No Patient Navigation (PN) + 30 DayPN-Engage0 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 10 DayPN-Engage2 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 30 DayPN-Engage2 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 10 DayPN-Engage0 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 30 DayPN-Engage0 Participants
Text Message (TM) + Patient Navigation (PN) + 10 DayPN-Engage2 Participants
Text Message (TM) + Patient Navigation (PN) + 30 DayPN-Engage0 Participants
Secondary

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.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 DayPN-Request0 Participants
Conversational Agent (CA) + No Patient Navigation (PN) + 30 DayPN-Request0 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 10 DayPN-Request3 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 30 DayPN-Request3 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 10 DayPN-Request0 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 30 DayPN-Request0 Participants
Text Message (TM) + Patient Navigation (PN) + 10 DayPN-Request3 Participants
Text Message (TM) + Patient Navigation (PN) + 30 DayPN-Request1 Participants
Secondary

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]

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 DayReach-Engage Testing90 Participants
Conversational Agent (CA) + No Patient Navigation (PN) + 30 DayReach-Engage Testing73 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 10 DayReach-Engage Testing78 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 30 DayReach-Engage Testing68 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 10 DayReach-Engage Testing155 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 30 DayReach-Engage Testing154 Participants
Text Message (TM) + Patient Navigation (PN) + 10 DayReach-Engage Testing171 Participants
Text Message (TM) + Patient Navigation (PN) + 30 DayReach-Engage Testing145 Participants
Secondary

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.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conversational Agent (CA) + No Patient Navigation (NoPN) + 10 DaySelf-reported Testing18 Participants
Conversational Agent (CA) + No Patient Navigation (PN) + 30 DaySelf-reported Testing16 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 10 DaySelf-reported Testing13 Participants
Conversational Agent (CA) + Patient Navigation (PN) + 30 DaySelf-reported Testing13 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 10 DaySelf-reported Testing32 Participants
Text Message (TM) + No Patient Navigation (NoPN) + 30 DaySelf-reported Testing37 Participants
Text Message (TM) + Patient Navigation (PN) + 10 DaySelf-reported Testing41 Participants
Text Message (TM) + Patient Navigation (PN) + 30 DaySelf-reported Testing25 Participants

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026