Advanced Health Information Technologies to Engage Parents, Clinicians, and Community Nutritionists in Coordinating Responsive Parenting Care: Descriptive Case Series of the Women, Infants, and Children Enhancements to Early Healthy Lifestyles for Baby (WEE Baby) Care Randomized Controlled Trial

Background Socioeconomically disadvantaged newborns receive care from primary care providers (PCPs) and Women, Infants, and Children (WIC) nutritionists. However, care is not coordinated between these settings, which can result in conflicting messages. Stakeholders support an integrated approach that coordinates services between settings with care tailored to patient-centered needs. Objective This analysis describes the usability of advanced health information technologies aiming to engage parents in self-reporting parenting practices, integrate data into electronic health records to inform and facilitate documentation of provided responsive parenting (RP) care, and share data between settings to create opportunities to coordinate care between PCPs and WIC nutritionists. Methods Parents and newborns (dyads) who were eligible for WIC care and received pediatric care in a single health system were recruited and randomized to a RP intervention or control group. For the 6-month intervention, electronic systems were created to facilitate documentation, data sharing, and coordination of provided RP care. Prior to PCP visits, parents were prompted to respond to the Early Healthy Lifestyles (EHL) self-assessment tool to capture current RP practices. Responses were integrated into the electronic health record and shared with WIC. Documentation of RP care and an 80-character, free-text comment were shared between WIC and PCPs. A care coordination opportunity existed when the dyad attended a WIC visit and these data were available from the PCP, and vice versa. Care coordination was demonstrated when WIC or PCPs interacted with data and documented RP care provided at the visit. Results Dyads (N=131) attended 459 PCP (3.5, SD 1.0 per dyad) and 296 WIC (2.3, SD 1.0 per dyad) visits. Parents completed the EHL tool prior to 53.2% (244/459) of PCP visits (1.9, SD 1.2 per dyad), PCPs documented provided RP care at 35.3% (162/459) of visits, and data were shared with WIC following 100% (459/459) of PCP visits. A WIC visit followed a PCP visit 50.3% (231/459) of the time; thus, there were 1.8 (SD 0.8 per dyad) PCP to WIC care coordination opportunities. WIC coordinated care by documenting RP care at 66.7% (154/231) of opportunities (1.2, SD 0.9 per dyad). WIC visits were followed by a PCP visit 58.9% (116/197) of the time; thus, there were 0.9 (SD 0.8 per dyad) WIC to PCP care coordination opportunities. PCPs coordinated care by documenting RP care at 44.0% (51/116) of opportunities (0.4, SD 0.6 per dyad). Conclusions Results support the usability of advanced health information technology strategies to collect patient-reported data and share these data between multiple providers. Although PCPs and WIC shared data, WIC nutritionists were more likely to use data and document RP care to coordinate care than PCPs. Variability in timing, sequence, and frequency of visits underscores the need for flexibility in pragmatic studies. Trial Registration ClinicalTrials.gov NCT03482908; https://clinicaltrials.gov/ct2/show/NCT03482908 International Registered Report Identifier (IRRID) RR2-10.1186/s12887-018-1263-z


Introduction
Most lower-income children in the United States receive frequent preventive care, with up to 7 visits in the first 6 months after birth from primary care providers (PCPs) and the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) [1][2][3]. Fragmentation across care settings can lead to inconsistent prevention messages and caregiver confusion [4]. A solution to coordinate care among parents, clinicians, and community health professionals is needed [4]. Stakeholders are aligned in their support of a solution that both personalizes messaging to meet parents' time-sensitive needs on infant development and integrates relevant data to coordinate care across settings and break down silos [4]. The perceived benefits of personalization, integration, and care coordination, according to stakeholders, include improved child health outcomes and reduced duplication of efforts [4].
From a preventive health model perspective, the need to collect and share data among patients and clinical and community health professionals aligns with a series of reports [5][6][7][8][9] calling for systems approaches through the integration and coordination of care across service settings [9,10]. Integrated and coordinated care approaches are commonly applied within the clinical sector [11][12][13] (eg, general physicians and specialists), but given the capabilities and demonstrated benefits of advanced health information technologies (HITs) [12,13], the contemporary calls aim to extend these approaches to public health, community settings, and patients. In particular, the Chronic Care Model and the Culture of Health Action Framework emphasize connectivity and integration of public health, clinical services, and social services to advance quality, health outcomes, and equity, specifically for vulnerable populations [14,15].
The integrated and coordinated care model described in this paper applied advanced HIT strategies and represents a novel cross-sector care delivery model to address patient-centered care [11,16]. As little is known about the feasibility of cross-sector delivery models, this study addresses a gap by applying and evaluating the usability of advanced HIT capabilities to engage patients and clinical and community providers in a broader patient-centered, integrated, and coordinated care process. The intervention arm of the WIC Enhancements to Early Healthy Lifestyles for Baby (WEE Baby) Care Study aimed to integrate and coordinate care on responsive parenting (RP) guidance related to feeding, sleep, and play. The intervention was based on an evidence-based program that included messages that mothers believe should be a part of pediatric or WIC care [17][18][19]. The objective of this paper is to demonstrate the usability of advanced HIT strategies designed to engage parents in reporting RP practices, integrate data into electronic records to inform and facilitate documentation of provided RP care, and share data between settings to facilitate coordination of care between PCPs and WIC. The findings are intended to inform and advance novel cross-sector delivery models conceptualized to improve patient-centered care and health outcomes. While health outcomes are beyond the scope of this paper, these findings will inform the feasibility of models that align organizational resources and integrate activities for collective impact on population health objectives.

Study Design
The integrated and care coordination delivery model was constructed for the WEE Baby Care Study, which has been described elsewhere [20]. Briefly, the WEE Baby Care Study was a pragmatic trial to modify maternal parenting practices, with the goal of preventing rapid infant weight gain and obesity. Mothers and their newborn infants were assigned to either a 6-month RP intervention group (n=131) that included advanced HIT strategies to integrate and coordinate care between pediatric PCPs and WIC nutritionists or a control group (n=157) receiving standard care [20]. This analysis is limited to the 131 mother-infant dyads who were enrolled in the intervention group in which advanced HIT strategies were applied to collect patient-reported data, use these data to inform patient-centered care, securely share data, and coordinate care between PCPs and WIC nutritionists.

Participants and Recruitment
From July 2016 to May 2018, mother-infant dyads were recruited and enrolled from northeastern Pennsylvania, an area characterized by the Health Services and Resources Administration as medically underserved, with shortages in health, dental, and mental health professionals [21]. Mother-infant dyads were either recruited in person in the labor and delivery unit or on the phone after the first well-child visit (WCV). Eligible dyads met the following inclusion criteria: full-term (≥37 weeks gestation) infant, singleton newborn, English-speaking mother between 18 and 55 years old, intention to receive well-child care at a participating pediatric clinic, and eligibility to be enrolled in or current enrollment in WIC. Participants provided written informed consent. All study procedures were approved by the institutional review boards of The Pennsylvania State University and Geisinger.

Intervention and Advanced HIT Strategies
Mother-infant dyads randomized into the intervention group completed the Early Healthy Lifestyles (EHL) risk assessment tool prior to each WCV. The study team developed the EHL risk assessment tool to facilitate mothers' self-assessments of their RP practices related to feeding, soothing, and playing with the infant, as well as the infant's sleep behaviors. The parent was prompted by electronic messaging to complete the EHL in the patient portal prior to the WCV. The mother's proxy access to the child's portal was ensured at study enrollment. If the parent did not complete the tool, clinic staff encouraged the parent to complete the EHL in the waiting room on a tablet. Parent responses were then instantly integrated into the infant's electronic health record (EHR) (Epic Systems).
Within the WCV progress note, PCPs could view and use the EHL data to inform and document patient-centered RP care. Prior to the start of the intervention, participating PCPs were trained to evaluate the EHL data, deliver tailored RP messages that aligned with parent learning needs at WCVs, and document provided RP care in the study-specific table in the WVC progress note, herein referred to as the PCP system. Age-appropriate, preventive messages were informed by the Intervention Nurses Start Infants Growing Healthy Trajectories (INSIGHT) study and American Academy of Pediatrics Healthy Active Living for Families curriculum [17,22,23]. PCPs used progress note functions to facilitate documentation of RP care provided during the WCV. Additionally, PCPs could add an 80-character, free-text comment to send to the WIC nutritionist, perhaps to direct attention to a high-priority issue. No action by the PCP was required to initiate data sharing. Development of the PCP system was guided, approved, and integrated into the EHR by Geisinger's Health Information Technology Team.
Advanced HIT strategies were used to automate and securely share data of interest (Textbox 1) from the PCP to WIC, including parent EHL responses, PCP documentation of RP care, and child physical assessment. In turn, these data were automatically integrated and displayed in a study-specific system (herein referred to as the WIC system) to inform patient-centered counseling as coordinated care in the community setting. The WIC system was separate from WIC's standard electronic participant management system-QuickWIC, a HTML system developed in the late 1990s-and could be used in parallel. Separate log-ins were required for each system. WIC nutritionists documented RP care in QuickWIC and comments in the WIC system. The WIC system extracted education codes from QuickWIC. Following the visit with the trained WIC nutritionist, encounter data of interest (Textbox 1) were extracted from the WIC system and securely shared from WIC to the PCP, thus providing a communication feedback loop to coordinate care at subsequent visits. Uniquely, the WIC system required the nutritionist to sign off on the record after the visit was completed to initiate data sharing. WIC nutritionists received training on this process, the use of EHL data, and the delivery of RP care messages prior to the start of the intervention. A booster training session was provided in the 14th month of the intervention. Data were exchanged between the PCP system and the WIC system through a secure file transport portal managed by the clinical care setting study team, and data were refreshed on weekdays. This process continued for a 6-month period to allow multiple opportunities for care coordination using shared data across clinic and community settings. Figure 1 provides an overview of the flow for patient-reported data collection, integration, sharing, and care coordination. An application developer at the Pennsylvania Department of Health developed and implemented the WIC system as an external cloud system as opposed to an integrated system, as statewide plans were underway to replace the QuickWIC system.
Attendance of WCVs and WIC visits was not mandatory or incentivized in this pragmatic study but was necessary for data of interest to be collected. The typical WCV schedule for infants within the health system includes visits at 3 to 5 days (newborn), 1 month, 2 months, 4 months, and 6 months of age. The study team expected that the intervention participants would attend at least 4 WCVs. To receive WIC benefits, infants and their mothers enrolled in WIC need to have a visit every 3 months; thus, the study team expected intervention participants would attend at least 2 WIC visits. In sum, this would allow multiple opportunities for care coordination between PCPs and WIC. Textbox 1. Existing and study-specific systems with associated data elements shared by pediatric primary care providers from well-child visits and the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) nutritionists from appointments to inform care coordination. Italics indicate essential data elements for data set used for coding of data sharing, care coordination opportunity, and care coordination. Infant date of birth and enrollment date were extracted from the research team's records.

Data from pediatric clinics
Existing electronic health record:

Outcome Definitions
The outcomes of interest included the use of the advanced HIT strategies and the feasibility of data sharing and care coordination occurring in 2 directions, from PCPs to WIC and from WIC to PCPs. Data sharing is the electronic and systematic push of study-related data through the electronic data warehouse (distinct from the EHR and PCP system) managed by the research team in the clinical setting. Data sharing does not require the PCP or WIC nutritionist in the receiving setting to interact with the data of interest (Textbox 1).
A care coordination opportunity is nested within data sharing and is an opportunity for a PCP or WIC nutritionist to view data for the most recent visit from the sending setting. Due to the secure and study staff-dependent data sharing processes, the receiving provider was able to view the shared data within 2 business days if sent by the PCP and 1 business day if sent by the WIC nutritionist. Eligible WCVs occurred after the dyad was enrolled into the study and continued up to 6 months of the infant's age, at which time the clinical study team turned off the PCP system. Eligible WIC visits occurred after the dyad was enrolled in the study but before disabling the PCP system.
Care coordination is nested within a care coordination opportunity and requires a PCP or WIC nutritionist in the receiving setting to be able to access the sent data and document the provided RP care. The study team could not directly verify that the receiving setting interacted with the sent data, as accessing or viewing the data was not captured with a discrete data point; thus, the documentation of RP care serves as proxy evidence that the receiving provider used the shared data to coordinate care. Preventive RP care included educational messages that addressed parent learning needs as self-assessed by parents using the EHL tool. Preventive RP care was documented by PCPs and WIC nutritionists by selecting RP topics, writing a free-text comment, or both.

Coding of Outcomes
The coding process was operationally detailed in a study team-developed coding manual that was extensively reviewed multiple times by 5 study team members (SMRK, HAH, MM, JSS, and LBD) and applied to a comprehensive, single data set. The data set included data from the PCP system and the WIC system along with other data elements listed in Textbox 1 to identify data sharing, care coordination opportunities, and care coordination outcomes. Two postdoctoral-level study team members (SMRK and HAH) coded the data independently, discrepancies were discussed and resolved using the coding manual, and both team members recoded the discrepant observations. After the first round of coding, 86% of coded observations agreed between the two coders, demonstrating adequate understanding of the coding process. This process continued until the 2 sets of coded data completely matched.
PCP to WIC data sharing, care coordination opportunities, and care coordination events were identified. The criteria for these outcomes are depicted in Figure 2. PCP to WIC data sharing required an eligible WCV to have at least one of the following data points documented: (1) parent-completed EHL, (2) documentation of RP care provided by the PCP, (3) PCP comment to WIC, (4) immunization records, or (5) weight and length. After the identified PCP to WIC data sharing occurrence, a PCP to WIC care coordination opportunity occurred when the WCV was followed by an eligible WIC visit that occurred two or more business days after the WCV to allow ample time for the shared data to be available in the WIC system for the nutritionist. Subsequently, a PCP to WIC care coordination event was identified when the WIC nutritionist documented provided RP care or commented to the PCP and signed off on the record. WIC to PCP data sharing, care coordination opportunities, and care coordination events were identified. As shown in Figure  3, WIC to PCP data sharing occurred when an eligible WIC visit had (1) documentation of RP care provided by the nutritionist or (2) a nutritionist comment or comments to the PCP, in addition to (3) a nutritionist sign-off on the same day or after the WIC visit. After the identified WIC to PCP data sharing occurrence, a WIC to PCP care coordination opportunity was identified when the WIC sign-off date was directly followed by a WCV to allow for shared data to be available in the PCP system for the PCP. Subsequently, a WIC to PCP care coordination event was identified when the PCP documented EHL-related preventive counseling or commented to WIC on the same day as the WCV.

Statistical Analysis
All data were processed and analyzed using SAS (version 9.4; SAS Institute Inc). The SAS functions "Proc Freq" and "Proc Means" were used to describe the sample and determine the total number and mean per dyad (with standard deviation) of variables of interest to describe the usability of the advanced HIT technologies and feasibility of data sharing and care coordination using the coded variables described above.

Participants
As shown in Table 1

Discussion
This study suggests that advanced HIT strategies are a potential solution to engage parents in reporting RP practices, integrate data into the infant's electronic patient management systems to inform and facilitate documentation of provided RP care, and share data between PCPs and WIC nutritionists serving socioeconomically disadvantaged parents and infants from an area with known shortages in health care services. Even though bidirectional data sharing was feasible, care coordination occurred less frequently. Typically, these advanced HIT strategies are commonly found and siloed in larger health systems with standardized EHRs, a resource supported by policy and practice [11][12][13]; however, the current study applied advanced HIT strategies to bidirectionally share data across local community and clinical settings, an important step in coordinating patient-centered preventive care. Implemented strategies used to collect, integrate, and share data were adopted by patients, PCPs, and WIC nutritionists, suggesting usability, but variable utilization of certain components inhibited care coordination. Replication and dissemination of a cross-sector model may be facilitated by clinical partners practicing in a standardized EHR environment, with these findings providing foundational lessons and recommendations for future iterations.
Observed data sharing between clinic and community settings demonstrated usability, yet PCP to WIC data sharing occurred at more than twice the rate of WIC to PCP data sharing, likely mirroring the more frequently scheduled and attended WCVs relative to WIC visits. The infrastructure and processes developed to share data between PCPs and WIC differed in reliability and efficiency. PCP to WIC data sharing functioned more reliably than in the reverse direction. Data elements were passively extracted from EHRs without PCP action beyond standard documentation and thus were reliably (459/459, 100%) shared with WIC after the WCVs. In comparison, WIC to PCP data sharing was less reliable (197/296, 66.6%), as the process required the WIC nutritionist to sign off in the WIC system, a step that was missed for one-third of events, impacting usability. In addition, this extra step in the nutritionists' workflow was critical for PCP to WIC care coordination, as a sign-off on the WIC system was required to complete the coordination process with the PCP. This suggests that processes that change standard workflow or require an additional step may inhibit data sharing from the community setting. However, passive HIT strategies to collect and extract data can feasibly and effectively facilitate data sharing from a clinical to a nonclinical setting; thus, future iterations of this model should use passive, automatic processes in both settings.
Although WIC to PCP data sharing was less effective, the process was more efficient than in the reverse direction. The WIC to PCP data sharing process took 1 business day and was dependent on human resources. After the WIC nutritionist signed off of the WIC system, data were extracted that evening and sent to the research team in the clinical setting via a secure file transport portal and then integrated into the infant's EHR by a research team staff member the next morning. In contrast, after data were extracted from the EHR the morning after a WCV, data were sent via a secure file transport portal to a centralized team member at WIC, who uploaded the data to the WIC system, which refreshed at midnight via an automatic batch process. Thus, the process for PCP to WIC data sharing was 2 business days and was also human dependent. Due to staff availability in both the clinical research and central WIC settings, all data transfer steps were delayed by holidays and staff absences, planned and unplanned. Even though the data sharing process between PCPs and WIC was completed in 1 to 2 business days, future applications should aim to shorten this delay and automate the data transfer in real time. Addressing these limitations would accommodate participants who attend multiple visits within the same day or on consecutive days and reduce reliance on human resources, thus increasing the generalizability of the model to real-world settings with limited resources.
Care coordination was seldomly observed, in part due to the limitations of the data sharing processes, the wide variation in the attendance (frequency and pattern) of both WCVs and WIC visits, and the limited adoption of Low adoption of the documentation features of the PCP system may be due to variations in PCP practice that limited exposure to the system. Infants were randomized at the individual level as opposed to the PCP or clinic level. Thus, a PCP provided well-child care to infants in the treatment group (with the PCP system) and control group (without the PCP system), as well as to infants not involved in the study (without the PCP system) throughout the 22-month study period, creating inconsistencies in workflow and exposure to the PCP system. Out of the 459 WCVs attended by intervention dyads, PCPs documented RP preventive education at 162 (35.3%) visits. Documentation of RP preventive education, however, was a proxy for PCP system use and did not capture if the PCP viewed the EHL assessment tool or data from WIC within the PCP system and documented education elsewhere, such as the WCV note. Adoption of interventional EHR components may be improved through randomization at the PCP level, longer exposure times to innovations, additional training and booster sessions, feedback on performance, and enhanced organizational factors, such as administrative and operational support [24,25].
High adoption of RP care by WIC nutritionists may reflect strong alignment with their focused program goals and requirements [1]. This is evidenced by the high frequency of documented RP care in participant WIC records. Documentation of RP care was facilitated by using standard WIC education codes and integrating study team-created codes into WIC's standard electronic system (QuickWIC). Further, at some WIC visits, nutritionists could use parent-reported EHL data available to inform care. However, parent completion of EHL and the required cadence for a PCP to WIC care coordination opportunity (ie, a WCV followed by a WIC visit) limited the availability of EHL data to the nutritionist to a single event per dyad. Even though EHL data were available at about half of WIC visits, nutritionists provided and documented EHL-related RP education at most visits with dyads. In comparison, PCPs comprehensively assess and address growth, development, and safety issues at WCVs but perceive WIC nutritionists as having more time to discuss important nutrition and feeding issues and predicted clear benefits in cross-sector integration and coordination [4]. Thus, sharing nutritionists' documentation of preventive counseling may provide opportunities for the PCP to coordinate care by allowing the brief reinforcement of messages or time to discuss new or other topics pertinent to the care of their patient.
The study demonstrated that HIT strategies can facilitate the collection, integration, and sharing of patient-reported data on parenting practices in 2 settings. Most parents routinely completed the EHL 2 or more times, and PCPs had access to parent-reported EHL data at about half of the visits, which was then shared with WIC nutritionists to view at more than half of the care coordination opportunities. Parent responses to the EHL were automatically integrated into the infant's electronic health record in the pediatric setting and into the study-specific WIC system to prompt PCPs and WIC nutritionists to provide tailored RP counseling. Integrating parent-reported data into health care professionals' workflow and electronic patient management system prior to a visit may lead to patient-centered care by highlighting timely concerns and streamlining patient assessment. However, electronic solutions to collect patient-reported information need to account for technology availability at both the patient and clinic levels so as to not exacerbate the digital divide seen between lower-and higher-income populations [26].
Reliance on human resources for data sharing impacted the reliability and efficiency of processes to transfer data between clinical and community settings to facilitate care coordination; however, the system developed for this study addressed stakeholder concerns related to security of data sharing across settings [4]. Importantly, given the imperative of protecting patient rights and the health system's responsibility to maintain privacy, patient consent to share a limited data set across settings is warranted [4,16,27]. Executing interinstitutional agreements between the community and clinical settings for limited data sharing with participant consent was a critical and substantial step in the development of data sharing processes and addressed stakeholder concerns. In addition, using in-person or over-the-phone staff recruitment to obtain participant consent using paper or electronic consent forms, as well as the use of a secure file transport portal, addressed privacy concerns related to the Health Insurance Portability and Accountability Act and data security [4]. Further innovations in HIT strategies are needed to more efficiently and effectively share limited patient data sets with aligned community and public health agencies to address limitations related to workflow, human resources, and timeliness. Within the clinical sector, HIT strategies have been used to facilitate efficient data exchange between providers, and technologies are emerging for data exchange between clinical and public health settings [28,29]. Pairing these HIT technologies with strategies for data integration, as described here, presents a rich opportunity for scaling cross-sector data sharing into practice in order to implement recommendations from integrated and coordinated care models, achieving collective impact and advancing population health objectives [9,15].
While a strength of the pragmatic study is the observation of real-life patterns of care, a limitation to testing care coordination was that few participants completed the expected 4 WCVs or 2 WIC visits in a 6-month observation period. Visit attendance, timing, and the sequence of visit types was not determined or controlled by the study team. Socioeconomically disadvantaged parents and infants experience many barriers to attending WIC appointments, including lack of transportation or childcare, conflicting activities, negative feelings about nutrition education, and frequent relocation [30]. Research in the prenatal period suggests that providing low-income additional supports, such as case managers or outreach and community health care workers [31], may enhance efforts to coordinate care between clinical and community settings by promoting timely visit attendance. Although WEE Baby Care was informed by a formative qualitative phase that captured the perceptions of stakeholders, including PCPs, WIC nutritionists, and parents [4], the perspectives of these stakeholders on the implementation of the intervention components were not captured, which limited our understanding of how PCPs and nutritionists integrated the intervention into their workflow. Additional training booster sessions and a longer intervention period may have improved adoption of the PCP and WIC systems through reminders and increased exposure. Further, the limitations of the WIC system and iterations of this model may be optimized, as WIC has implemented an updated, nationally standardized participant management system since the completion of this study, providing an opportunity to improve the technology as well as the potential for evaluation and spread. Recruiting dyads after the first WCV likely reduced the number of potential opportunities for data sharing and care coordination. Lastly, most of the participating low-income mothers were White, all were English speaking, and most had a high school diploma or higher. This was representative of the Geisinger region, but generalizability to the more diverse national WIC and low-income populations with lower educational attainment may be limited [32,33].
Advanced HIT strategies can share data across clinical and community settings, even in a socioeconomically disadvantaged area with shortages in health care services; however, improvements in the usability of key strategies are needed to facilitate care coordination and increase generalizability to other settings. In alignment with models calling for integration and care coordination across settings [9,15], this intervention employed a comprehensive set of advanced HIT strategies, including patient (parent) access to their infant's EHR (patient portal), patient (parent) electronic completion of a risk assessment that becomes integrated into their infant's EHR, secure data sharing mechanisms, the ability for PCPs and WIC nutritionists to communicate securely, system analytics to manage preventive care, and interoperability between clinical and community data systems [11,16]. Future research is needed to address process limitations affecting the reliability and effectiveness of data sharing and care coordination and the suboptimal use of health care services. Integrating clinical and community health care services through electronic data sharing with advanced HIT strategies could be an integral approach to providing coordinated, patient-centered health care to low-income, socioeconomically disadvantaged populations. and data collection. All authors have been involved in the critical revision of the manuscript and have given final approval to the submitted version.

Conflicts of Interest
None declared.