Childhood ObesityMW-PRCCRPNCT07479498
Mountain West Prevention Research Center Core Research Project
A study testing Text Message-based recruitment and Active outreach follow-up in people with Childhood Obesity, run by Paul Estabrooks at 1 site in United States.
Trial summary
This hybrid type 3 effectiveness-implementation sequential multiple assignment randomized trial will assess the impact of integrating population health management (PHM) strategies-text messaging and enrollment in Building Healthy Families (BHF)-for lower-income families with a child with obesity identified through… Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Childhood Obesity
- What is being tested?
- Text Message-based recruitment and Active outreach follow-up
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 600 participants
- Where
- 1 siteUnited States
- Study dates
- 30 Sep 2024to 29 Sep 2029
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Families
- Parent or legal caregiver and at least one child aged 5 to 12 years
- Child identified through electronic health record data from a participating clinical organization
- Child has had at least one clinical encounter at the participating site within the past 12 months
- Child has body mass index (BMI) at or above the 85th percentile for age and sex
- Caregiver has not opted out of receiving text communication from the clinic
Show all 13Show fewer
- Valid mailing address and telephone number listed in the electronic health record
- Parents and/or Caregivers
- Parent or legal caregiver of an eligible child
- Responsible for the child's care and able to provide consent for program participation
- Children
- Aged 5 to 12 years at time of identification
- Meet all criteria listed above
Who cannot join
- Child has a medical condition or contraindication that precludes participation in moderate physical activity
- Child has severe cognitive or physical impairment that would prevent participation in the intervention
- Child or family is currently participating in another structured weight management or obesity treatment program
- Family opts out of receiving study-related communications
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
The University of Utah
Salt Lake City, Utah, 84112
Madeleine L French, MS, 6166175034, madeleine.french@utah.edu
About this study
This hybrid type 3 effectiveness-implementation sequential multiple assignment randomized trial will assess the impact of integrating population health management (PHM) strategies-text messaging and enrollment in Building Healthy Families (BHF)-for lower-income families with a child with obesity identified through electronic health record (EHR) data. BHF promotes family healthy eating, physical activity, and lifestyle behavior strategies to manage weight. The research team will partner with clinical sites (community health clinics, pediatric clinics, rural hospitals) and Community-Based Organizations (CBOs). Clinical partners will execute data-sharing agreements enabling the research team to identify eligible children and caregivers and conduct outreach via text messaging. CBO partners will deliver BHF and provide de-identified data for program evaluation. Community Implementation Teams (CITs) will complete training, surveys, interviews, learning collaborative activities, fidelity assessments, and time tracking as part of quality improvement. The BHF Action Learning Collaborative will use quarterly sessions and Plan-Do-Study-Act cycles to address recruitment, implementation, sustainability, social determinants of health, and team coordination. The research team will record sessions, conduct direct observations of BHF delivery, and take field notes to assess fidelity and adaptations. Families will be identified through EHR records and mailed a consent and authorization cover letter, postcard, QR code, and intervention information with opt-out options. Those who do not opt out will be randomized to bidirectional text messaging with one-touch response and enrollment opportunities, with or without active outreach (telephone or text) from the local CIT. Enrolled families will complete orientation, baseline assessment, and weekly group sessions with ongoing follow-up. Attendance, body weight, goals, and self-monitoring will be recorded in a CIT data portal. Families will be randomized to receive either simple text reminders or reminders with motivational and skill-building prompts matched to session topics. CITs will also connect families to food assistance programs and local resources. Each CIT will complete two cohorts over two years. The primary outcome is reach; secondary outcomes include session attendance, changes in child BMI-z scores, changes in parent or caregiver weight, and changes in adoption, implementation, and maintenance at the community level.
Read the detailed description
The researchers propose a hybrid type 3 effectiveness-implementation sequential multiple assignment randomized trial (HEI-SMART) to determine the impact of integrating population health management (PHM) via text messaging and direct enrollment in Building Healthy Families (BHF) for lower-income families with a child aged 5-12 years with obesity identified through clinical partner (community health clinics, pediatric clinics, rural hospitals) electronic health record data. The sequential randomization design focuses on both initial recruitment (primary outcome) and retention in BHF sessions by randomly assigning enrolled families to text-only or text plus motivational retention messages.
BHF is a community-delivered evidence-based intervention to prevent and treat childhood obesity. The intervention educates families about healthy eating, physical activity, and healthy habits and facilitates goal setting and self-monitoring to improve lifestyle behaviors and manage weight. BHF includes a standard program evaluation conducted by community-based organizations (CBOs) to support quality improvement. The initial procedures describe activities undertaken by the research team to facilitate BHF delivery.
Identifying Community Partners An interdisciplinary network across the Mountain West region will provide infrastructure for applied research addressing obesity-related disparities among low-income families in rural and micropolitan communities in Idaho, Montana, Nevada, Utah, Wyoming, and surrounding states. This network will identify clinical organizations and CBOs to partner in identifying eligible patients and delivering BHF.
Clinical Organizations Participating clinical organizations will complete data-sharing agreements enabling PHM strategies to identify eligible children and caregivers through EHRs and conduct outreach via text messaging. Agreements permit study procedures to be conducted by the University of Utah research team, reducing burden on clinical partners.
The PHM strategy:
- Interfaces EHRs with a centralized cloud-based data warehouse
- Enables rapid cohort identification and messaging campaigns with patient-level randomization and bilingual messaging
- Supports bidirectional text messaging with single-touch response
- Provides a web-based dashboard for monitoring responses and supporting outreach The system is designed for potential use by other organizations with records of eligible families.
Community-Based Organizations CBO partners in corresponding geographic areas will deliver BHF. Enrolled families will be connected to local CBO programs. Data-sharing agreements will allow access to de-identified program evaluation data for secondary analysis.
Up to eight communities will be enrolled, adding two every six months beginning late in Year 1, through a standardized Request for Applications (RFA) process. Informational webinars disseminated through regional networks will describe BHF and application procedures. Communities will be selected based on:
- Demonstrated local need
- Capacity to deliver BHF
- Sustainability plans
- Likelihood of successful recruitment and implementation
Communities lacking required partnerships may apply for a partnership development award ($3,000) to build clinical collaborations, followed by a brief report and Organizational Readiness for Change survey after six months.
Community Implementation Teams Each CBO will establish a Community Implementation Team (CIT) including program, nutrition, physical activity, and lifestyle coordinators plus volunteers. Team composition is determined locally.
CIT members will receive access to the online BHF program platform and will complete electronic consent for evaluation activities including surveys, interviews, learning collaborative participation, lightning reports, and direct observations. BHF delivery follows the existing packaged intervention without modification.
Semi-Annual Surveys Surveys assessing training resources, facilitation, and context will be completed every six months beginning shortly after program access and continuing through six months after completion of a second cohort.
Program Package Engagement The package includes materials, training modules, knowledge checks, fidelity assessments, and a data portal, as well as screening for social needs. The Action Learning Collaborative will support development of community-specific plans addressing social determinants of health, particularly food insecurity.
Knowledge checks and fidelity assessments are embedded within the program, with de-identified aggregated data available to the research team.
Time Tracking CIT members will track activities associated with dissemination and implementation strategies using a web- or app-based system.
BHF Action Learning Collaborative CITs will participate in quarterly learning sessions and action periods following Plan-Do-Study-Act cycles addressing recruitment, readiness, engagement, implementation quality, sustainability, effectiveness, maintenance, social determinants of health, and coordination with clinical partners. Activities include synchronous sessions, on-demand support, and mid-quarter lightning reports to review progress and address barriers. Rapid qualitative analysis will inform action plans returned to CITs for ongoing improvement.
Sessions and technical interactions will be recorded, transcribed, and analyzed.
Direct Observations Observers will attend BHF sessions (1-18 per community) to assess fidelity using standardized checklists, attendance counts, and documentation of adaptations. Observers will minimize interaction and clarify that observations evaluate program delivery rather than individual performance.
Key Informant Interviews Semi-structured interviews with CIT members will assess strategies affecting RE-AIM outcomes and i-PARIHS constructs, including innovation characteristics, recipient factors, facilitation, and contextual influences.
Recruitment Procedures Text messaging content will be developed through iterative user-centered design with caregivers and community partners to ensure cultural and regional appropriateness and reduce stigma.
Participating clinical organizations will identify eligible families (child aged 5-12 years with BMI ≥85th percentile, recent clinical encounter, valid contact information, and permission for text contact). Families will receive mailed study information with multiple opt-out options including postcard, QR code form, telephone, or email.
Families not opting out within two weeks will be randomized to one of four outreach conditions:
- Single text invitation
- Single text plus active outreach
- Repeated texts over six months
- Repeated texts plus active outreach Messages will be bidirectional with one-touch response and enrollment links. Active outreach will consist of telephone contact from local CIT members.
Family Participation Interested families will enroll in BHF through local CBOs and complete orientation, consent, and baseline assessments including anthropometric measures, behavioral factors, and social determinants of health. Data will be stored in the BHF program portal.
Families will attend weekly two-hour group sessions for 12 weeks followed by ongoing sessions up to one year. Attendance, body weight, physical activity, nutrition, and self-monitoring will be recorded. Individual-level data will be obtained at 3, 6, and 12 months.
As part of the sequential design, enrolled families will be randomized to:
- Standard reminder texts
- Reminder texts plus motivational and skill-building messages Enhanced messages will target social cognitive theory constructs such as outcome expectations and self-efficacy and will align with session topics.
Resource Connection CITs will identify and connect families with community resources based on screening for needs, particularly food insecurity, using established guidance such as the PRAPARE toolkit. Strategies may include assistance with school meal programs, SNAP eligibility, and local food support services.
Each CBO will implement two cohorts over two years.
Outcomes The primary outcome is reach, defined as the proportion of interested families completing the BHF orientation session. Primary hypotheses compare recruitment effectiveness between single versus repeated text outreach.
Secondary outcomes include:
- Session attendance at 12 months
- Changes in child BMI-z scores
- Changes in parent or caregiver weight
- Adoption (number and proportion of communities delivering BHF)
- Implementation (proportion of activities completed by CITs)
- Maintenance (initiation of a third cohort)
- Conditions
- Childhood Obesity
- Being tested
- Text Message-based recruitment, Active outreach follow-up
- Keywords
- Family Healthy Weight Program, Population Health Management, Rural, Reach, Engagement
- Medical subject headings
- Pediatric Obesity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Text Message-based recruitmentBehavioural
Text messaging (TM) outreach delivered by the research team using bidirectional text messages sent to caregivers of eligible children identified through participating clinical organizations. Messages include a one-touch response option and a direct link to enroll in Building Healthy Families. Text messaging allows caregivers to respond directly to the community implementation team to express interest in enrollment. Participants may opt out of receiving messages at any time. Depending on the assigned study condition, participants may receive either a single outreach message or repeated outreach messages over a 3-month period.
Active outreach follow-upBehavioural
Active outreach (AO) consists of telephone or other follow-up contact with caregivers conducted by members of the local Community Implementation Team (CIT). During the call, CIT members provide information about the BHF, answer questions, and offer assistance with enrollment. Outreach scripts and approaches are adapted to the local community context to support engagement with eligible families. Active outreach represents a standard recruitment activity used by community partners to encourage participation in the program.
| Study group | Role | What they receive |
|---|---|---|
| TM-Single | Experimental | Participants receive a single bidirectional text message from the research team with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program. Receives: Behavioral: Text Message-based recruitment |
| TM-Single-AO | Experimental | Participants receive a single bidirectional text message from the research team with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program, plus telephone outreach from the local Community Implementation Team. Receives: Behavioral: Text Message-based recruitment; Behavioral: Active outreach follow-up |
| TM-Repeat | Experimental | Participants receive repeated bidirectional text messages from the research team over a 3-month period, with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program. Participants may opt out of receiving messages at any time. Receives: Behavioral: Text Message-based recruitment |
| TM-Repeat-AO | Experimental | Participants receive repeated bidirectional text messages from the research team over a 3-month period, with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program, plus telephone outreach from the local Community Implementation Team. Participants may opt out of receiving messages at any time. Receives: Behavioral: Text Message-based recruitment; Behavioral: Active outreach follow-up |
What is being measured
The primary outcome is the main question the study is designed to answer.
Reach: Enrollment in the Building Healthy Families Program
Reach is defined as the proportion of eligible families who enroll in the Building Healthy Families program following outreach through population health management strategies. Enrollment is operationalized as completion of the BHF orientation session after responding to text messaging and/or active outreach recruitment strategies. Reach will be compared across randomized recruitment strategies that vary by text message frequency (single vs repeated outreach) and the presence or absence of active telephone outreach from the Community Implementation Team.
Measured: Up to 3 months after initial outreach
Program Attendance (Participant Retention)
Attendance is defined as the proportion of scheduled BHF sessions attended by enrolled families during the program delivery period. Attendance data will be captured through the BHF program data portal and reflects ongoing engagement with the intervention following enrollment.
Measured: 12 months after enrollment
Secondary outcomes (5)
Child BMI z-score
Change in child BMI z-score measured from baseline to follow-up using anthropometric measurements collected during BHF program evaluation. BMI z-scores will be calculated based on standardized CDC growth charts for children.
Measured: Baseline, 3 months, and 12 months after enrollment.
Change in parent/caregiver weight
Change in parent or caregiver body weight measured from baseline to follow-up as part of the BHF program evaluation. Weight is collected during program sessions and recorded in the BHF data portal.
Measured: Baseline, 3 months, and 12 months after enrollment
Number of Communities Adopting Building Healthy Families
Adoption is defined as the number and proportion of rural and micropolitan communities that agree to implement and initiate delivery of the BHF program following the partnership development grant and request for applications process.
Measured: Up to 4 years
Direct observation of Implementation fidelity
Implementation fidelity is defined as the proportion of required program activities completed during BHF sessions as reported by Community Implementation Team members and assessed using session fidelity checklists embedded in the BHF program package.
Measured: Up to 12 months after program initiation
Number of Communities Maintaining BHF delivery
Maintenance is defined as the continued delivery of BHF beyond the initial cohort of families, operationalized as the initiation of a second or third cohort of BHF participants by a community implementation team.
Measured: Up to 24 months after program initiation.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Mar 2026
- Study start30 Sep 2024
- Primary completion29 Sep 2029 (estimated)
- Study completion29 Sep 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Childhood ObesityStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This hybrid type 3 effectiveness-implementation, sequential multiple assignment randomized trial (HEI-SMART) will test the impact of integrating PHM via text messaging and direct enrollment in Building Healthy Families (BHF) for lower-income families with a child (6-12 years) who has obesity, identified through community health center electronic health record data.
- Masking
- None (open label)
- Enrolment
- 600 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Paul Estabrooks
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Paul Estabrooks, University of Utah
- Investigators
- Paul A Estabrooks, PhD, Principal investigator, University of Utah
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07479498
- Sponsor's protocol ID
- U48DP006789
- Other IDs
- 1 U48DP006789-01-00
- Acronym
- MW-PRCCRP
- Status last verified
- Mar 2026
- First submitted
- 8 Mar 2026
- Last updated
- 18 Mar 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Deidentified, scored datasets for the primary outcome (reach) and secondary outcomes will be made available at the time of peer review publication and will be open access for 7 years following the end of the trial period.
Study at a glance
From the registry record, last updated by the sponsor on 18 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Mountain West Prevention Research Center Core Research Project
- ClinicalTrials.gov ID
- NCT07479498
- Acronym / sponsor ID
- MW-PRCCRP / U48DP006789
- Conditions
- Childhood Obesity
- Keywords
- Family Healthy Weight Program, Population Health Management, Rural, Reach, Engagement
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 600 participants (estimated)
- Lead sponsor
- Paul EstabrooksUniversity, hospital or other
- Study start
- 30 Sep 2024 (actual)
- Primary completion
- 29 Sep 2029 (estimated)
- Study completion
- 29 Sep 2029 (estimated)
- First posted
- 18 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This hybrid type 3 effectiveness-implementation sequential multiple assignment randomized trial will assess the impact of integrating population health management (PHM) strategies-text messaging and enrollment in Building Healthy Families (BHF)-for lower-income families with a child with obesity identified through electronic health record (EHR) data. BHF promotes family healthy eating, physical activity, and lifestyle behavior strategies to manage weight. The research team will partner with clinical sites (community health clinics, pediatric clinics, rural hospitals) and Community-Based Organizations (CBOs). Clinical partners will execute data-sharing agreements enabling the research team to identify eligible children and caregivers and conduct outreach via text messaging. CBO partners will deliver BHF and provide de-identified data for program evaluation. Community Implementation Teams (CITs) will complete training, surveys, interviews, learning collaborative activities, fidelity assessments, and time tracking as part of quality improvement. The BHF Action Learning Collaborative will use quarterly sessions and Plan-Do-Study-Act cycles to address recruitment, implementation, sustainability, social determinants of health, and team coordination. The research team will record sessions, conduct direct observations of BHF delivery, and take field notes to assess fidelity and adaptations. Families will be identified through EHR records and mailed a consent and authorization cover letter, postcard, QR code, and intervention information with opt-out options. Those who do not opt out will be randomized to bidirectional text messaging with one-touch response and enrollment opportunities, with or without active outreach (telephone or text) from the local CIT. Enrolled families will complete orientation, baseline assessment, and weekly group sessions with ongoing follow-up. Attendance, body weight, goals, and self-monitoring will be recorded in a CIT data portal. Families will be randomized to receive either simple text reminders or reminders with motivational and skill-building prompts matched to session topics. CITs will also connect families to food assistance programs and local resources. Each CIT will complete two cohorts over two years. The primary outcome is reach; secondary outcomes include session attendance, changes in child BMI-z scores, changes in parent or caregiver weight, and changes in adoption, implementation, and maintenance at the community level.
Detailed description
The researchers propose a hybrid type 3 effectiveness-implementation sequential multiple assignment randomized trial (HEI-SMART) to determine the impact of integrating population health management (PHM) via text messaging and direct enrollment in Building Healthy Families (BHF) for lower-income families with a child aged 5-12 years with obesity identified through clinical partner (community health clinics, pediatric clinics, rural hospitals) electronic health record data. The sequential randomization design focuses on both initial recruitment (primary outcome) and retention in BHF sessions by randomly assigning enrolled families to text-only or text plus motivational retention messages.
BHF is a community-delivered evidence-based intervention to prevent and treat childhood obesity. The intervention educates families about healthy eating, physical activity, and healthy habits and facilitates goal setting and self-monitoring to improve lifestyle behaviors and manage weight. BHF includes a standard program evaluation conducted by community-based organizations (CBOs) to support quality improvement. The initial procedures describe activities undertaken by the research team to facilitate BHF delivery.
Identifying Community Partners An interdisciplinary network across the Mountain West region will provide infrastructure for applied research addressing obesity-related disparities among low-income families in rural and micropolitan communities in Idaho, Montana, Nevada, Utah, Wyoming, and surrounding states. This network will identify clinical organizations and CBOs to partner in identifying eligible patients and delivering BHF.
Clinical Organizations Participating clinical organizations will complete data-sharing agreements enabling PHM strategies to identify eligible children and caregivers through EHRs and conduct outreach via text messaging. Agreements permit study procedures to be conducted by the University of Utah research team, reducing burden on clinical partners.
The PHM strategy:
- Interfaces EHRs with a centralized cloud-based data warehouse
- Enables rapid cohort identification and messaging campaigns with patient-level randomization and bilingual messaging
- Supports bidirectional text messaging with single-touch response
- Provides a web-based dashboard for monitoring responses and supporting outreach The system is designed for potential use by other organizations with records of eligible families.
Community-Based Organizations CBO partners in corresponding geographic areas will deliver BHF. Enrolled families will be connected to local CBO programs. Data-sharing agreements will allow access to de-identified program evaluation data for secondary analysis.
Up to eight communities will be enrolled, adding two every six months beginning late in Year 1, through a standardized Request for Applications (RFA) process. Informational webinars disseminated through regional networks will describe BHF and application procedures. Communities will be selected based on:
- Demonstrated local need
- Capacity to deliver BHF
- Sustainability plans
- Likelihood of successful recruitment and implementation
Communities lacking required partnerships may apply for a partnership development award ($3,000) to build clinical collaborations, followed by a brief report and Organizational Readiness for Change survey after six months.
Community Implementation Teams Each CBO will establish a Community Implementation Team (CIT) including program, nutrition, physical activity, and lifestyle coordinators plus volunteers. Team composition is determined locally.
CIT members will receive access to the online BHF program platform and will complete electronic consent for evaluation activities including surveys, interviews, learning collaborative participation, lightning reports, and direct observations. BHF delivery follows the existing packaged intervention without modification.
Semi-Annual Surveys Surveys assessing training resources, facilitation, and context will be completed every six months beginning shortly after program access and continuing through six months after completion of a second cohort.
Program Package Engagement The package includes materials, training modules, knowledge checks, fidelity assessments, and a data portal, as well as screening for social needs. The Action Learning Collaborative will support development of community-specific plans addressing social determinants of health, particularly food insecurity.
Knowledge checks and fidelity assessments are embedded within the program, with de-identified aggregated data available to the research team.
Time Tracking CIT members will track activities associated with dissemination and implementation strategies using a web- or app-based system.
BHF Action Learning Collaborative CITs will participate in quarterly learning sessions and action periods following Plan-Do-Study-Act cycles addressing recruitment, readiness, engagement, implementation quality, sustainability, effectiveness, maintenance, social determinants of health, and coordination with clinical partners. Activities include synchronous sessions, on-demand support, and mid-quarter lightning reports to review progress and address barriers. Rapid qualitative analysis will inform action plans returned to CITs for ongoing improvement.
Sessions and technical interactions will be recorded, transcribed, and analyzed.
Direct Observations Observers will attend BHF sessions (1-18 per community) to assess fidelity using standardized checklists, attendance counts, and documentation of adaptations. Observers will minimize interaction and clarify that observations evaluate program delivery rather than individual performance.
Key Informant Interviews Semi-structured interviews with CIT members will assess strategies affecting RE-AIM outcomes and i-PARIHS constructs, including innovation characteristics, recipient factors, facilitation, and contextual influences.
Recruitment Procedures Text messaging content will be developed through iterative user-centered design with caregivers and community partners to ensure cultural and regional appropriateness and reduce stigma.
Participating clinical organizations will identify eligible families (child aged 5-12 years with BMI ≥85th percentile, recent clinical encounter, valid contact information, and permission for text contact). Families will receive mailed study information with multiple opt-out options including postcard, QR code form, telephone, or email.
Families not opting out within two weeks will be randomized to one of four outreach conditions:
- Single text invitation
- Single text plus active outreach
- Repeated texts over six months
- Repeated texts plus active outreach Messages will be bidirectional with one-touch response and enrollment links. Active outreach will consist of telephone contact from local CIT members.
Family Participation Interested families will enroll in BHF through local CBOs and complete orientation, consent, and baseline assessments including anthropometric measures, behavioral factors, and social determinants of health. Data will be stored in the BHF program portal.
Families will attend weekly two-hour group sessions for 12 weeks followed by ongoing sessions up to one year. Attendance, body weight, physical activity, nutrition, and self-monitoring will be recorded. Individual-level data will be obtained at 3, 6, and 12 months.
As part of the sequential design, enrolled families will be randomized to:
- Standard reminder texts
- Reminder texts plus motivational and skill-building messages Enhanced messages will target social cognitive theory constructs such as outcome expectations and self-efficacy and will align with session topics.
Resource Connection CITs will identify and connect families with community resources based on screening for needs, particularly food insecurity, using established guidance such as the PRAPARE toolkit. Strategies may include assistance with school meal programs, SNAP eligibility, and local food support services.
Each CBO will implement two cohorts over two years.
Outcomes The primary outcome is reach, defined as the proportion of interested families completing the BHF orientation session. Primary hypotheses compare recruitment effectiveness between single versus repeated text outreach.
Secondary outcomes include:
- Session attendance at 12 months
- Changes in child BMI-z scores
- Changes in parent or caregiver weight
- Adoption (number and proportion of communities delivering BHF)
- Implementation (proportion of activities completed by CITs)
- Maintenance (initiation of a third cohort)
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 4
- Model description
- This hybrid type 3 effectiveness-implementation, sequential multiple assignment randomized trial (HEI-SMART) will test the impact of integrating PHM via text messaging and direct enrollment in Building Healthy Families (BHF) for lower-income families with a child (6-12 years) who has obesity, identified through community health center electronic health record data.
| Arm | Type | Receives |
|---|---|---|
| TM-Single | Experimental | Behavioral: Text Message-based recruitmentParticipants receive a single bidirectional text message from the research team with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program. |
| TM-Single-AO | Experimental | Behavioral: Text Message-based recruitment, Behavioral: Active outreach follow-upParticipants receive a single bidirectional text message from the research team with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program, plus telephone outreach from the local Community Implementation Team. |
| TM-Repeat | Experimental | Behavioral: Text Message-based recruitmentParticipants receive repeated bidirectional text messages from the research team over a 3-month period, with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program. Participants may opt out of receiving messages at any time. |
| TM-Repeat-AO | Experimental | Behavioral: Text Message-based recruitment, Behavioral: Active outreach follow-upParticipants receive repeated bidirectional text messages from the research team over a 3-month period, with a one-touch response option and a direct link to enroll in the Family Healthy Weight Program, plus telephone outreach from the local Community Implementation Team. Participants may opt out of receiving messages at any time. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (13 listed)
- Families
- Parent or legal caregiver and at least one child aged 5 to 12 years
- Child identified through electronic health record data from a participating clinical organization
- Child has had at least one clinical encounter at the participating site within the past 12 months
- Child has body mass index (BMI) at or above the 85th percentile for age and sex
Key exclusion criteria (4 listed)
- Child has a medical condition or contraindication that precludes participation in moderate physical activity
- Child has severe cognitive or physical impairment that would prevent participation in the intervention
- Child or family is currently participating in another structured weight management or obesity treatment program
- Family opts out of receiving study-related communications
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Text Message-based recruitmentText messaging (TM) outreach delivered by the research team using bidirectional text messages sent to caregivers of eligible children identified through participating clinical organizations. Messages include a one-touch response option and a direct link to enroll in Building Healthy Families. Text messaging allows caregivers to respond directly to the community implementation team to express interest in enrollment. Participants may opt out of receiving messages at any time. Depending on the assigned study condition, participants may receive either a single outreach message or repeated outreach messages over a 3-month period. | Behavioural | TM-Repeat, TM-Repeat-AO, TM-Single, TM-Single-AO |
| Active outreach follow-upActive outreach (AO) consists of telephone or other follow-up contact with caregivers conducted by members of the local Community Implementation Team (CIT). During the call, CIT members provide information about the BHF, answer questions, and offer assistance with enrollment. Outreach scripts and approaches are adapted to the local community context to support engagement with eligible families. Active outreach represents a standard recruitment activity used by community partners to encourage participation in the program. | Behavioural | TM-Repeat-AO, TM-Single-AO |
Primary outcome
Reach: Enrollment in the Building Healthy Families Program
Time frame: Up to 3 months after initial outreach
Reach is defined as the proportion of eligible families who enroll in the Building Healthy Families program following outreach through population health management strategies. Enrollment is operationalized as completion of the BHF orientation session after responding to text messaging and/or active outreach recruitment strategies. Reach will be compared across randomized recruitment strategies that vary by text message frequency (single vs repeated outreach) and the presence or absence of active telephone outreach from the Community Implementation Team.
Program Attendance (Participant Retention)
Time frame: 12 months after enrollment
Attendance is defined as the proportion of scheduled BHF sessions attended by enrolled families during the program delivery period. Attendance data will be captured through the BHF program data portal and reflects ongoing engagement with the intervention following enrollment.
5 secondary outcomes
Child BMI z-score
Time frame: Baseline, 3 months, and 12 months after enrollment.
Change in parent/caregiver weight
Time frame: Baseline, 3 months, and 12 months after enrollment
Number of Communities Adopting Building Healthy Families
Time frame: Up to 4 years
Direct observation of Implementation fidelity
Time frame: Up to 12 months after program initiation
Number of Communities Maintaining BHF delivery
Time frame: Up to 24 months after program initiation.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Mar 2026.
- Individual participant dataSharing planned: Yes. Deidentified, scored datasets for the primary outcome (reach) and secondary outcomes will be made available at the time of peer review publication and will be open access for 7 years following the end of the trial period.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Paul A Estabrooks, PhD principal investigator
University of Utah
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Text Message-based recruitment and Active outreach follow-up in people with Childhood Obesity, run by Paul Estabrooks at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 13 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 18 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Madeleine L French, MS (6166175034, madeleine.french@utah.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Reach: Enrollment in the Building Healthy Families Program (time frame: Up to 3 months after initial outreach). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2026.