Chronic Disease

62

Review clinical trials related to Chronic Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Taining Golden Lake Comprehensive Chronic Disease Management Initiative

This study aims to establish the first county-level, population-based prospective cohort in Taining County, Fujian Province, China. The cohort will include at least 20,000 residents aged 18 years or older. The project will systematically collect questionnaires, physical measurements, laboratory tests, imaging data, and biological samples to build a multi-dimensional health database and biobank. Through 3-year follow-up, the study seeks to reveal the epidemiological patterns and risk factors of chronic diseases, characterize the natural course of multimorbidity and aging syndromes, and develop a comprehensive chronic disease management model suitable for rural and mountainous regions.

Participants needed: 20,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: First Affiliated Hospital of Fujian Medical UniversityUpdated: Oct 6, 2026Locations: 1
Eligibility criteria

Age ≥18 years, male or female. [+4]

Refusal to sign informed consent. [+4]

Status: Recruiting

AI-Assisted Personalized Heat-Risk Alerts

This two-arm randomized controlled trial will evaluate whether an artificial intelligence-assisted personalized heat-risk alert system reduces heat-related illness symptom burden among adults with chronic conditions. The intervention will integrate prespecified clinical characteristics with the Pakistan Meteorological Department's same-day forecast maximum temperature to classify individual heat-related acute clinical-event risk and deliver personalized alerts through a mobile application. The control group will receive a generic PMD heat-health advisory through the same application.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: National University of Medical Sciences, PakistanUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older attending the outpatient department of the selecte... [+5]

Patients requiring immediate emergency treatment or hospital admission at the ti... [+6]

Status: Not yet recruiting

Virtual Outreach and Individualized Coaching Extension

This study tests whether a nurse-led program that uses a voice-controlled smart speaker in the home helps older adults better manage their chronic health conditions. It also examines which nursing staff and clinic resources would be needed to offer such a program in regular outpatient care.

Participants needed: 50
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Emory UniversityUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Age 65 years or older [+7]

Diagnosis of Alzheimer's disease or a related dementia [+6]

Status: Recruiting

A Long-term Observational Study to Describe the Use of Vitamin-C Injektopas® 7.5 g in Patients With Vitamin C Deficiency

The goal of this observational study is to learn more about the disease and the symptoms where the product will use and in which patient groups. Further on, it is interesting to know clinical pictures, the symptoms improve. Patients with acute or chronical disease with vitamin c deficiency could be involved. The main questions it aims to answer are: * how do the symptoms of the disease change * how is the tolerability

Participants needed: 1,000
Trial details
Age: 18-120Biological sex: AllType: ObservationalSponsor: Pascoe Pharmazeutische Praeparate GmbHUpdated: Sep 17, 2026Locations: 1
Eligibility criteria

Patients with vitamin C deficiency [+1]

Hypersensitivity to the active ingredient or any of the excipients [+5]

Status: Recruiting

Improving the Collaborative Health of Adult Dyads

This study tests the efficacy of a dyadic intervention to mitigate the adverse health consequences of adults with pre-existing chronic health conditions and their informal carepartners (IC). Socioeconomically disadvantaged, older, and people from rural regions are more likely burdened with greater rates of chronic diseases such as diabetes, hypertension, chronic kidney disease, cardiovascular disease, and stroke.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of South CarolinaUpdated: Sep 18, 2026Locations: 1
Eligibility criteria

Male and female [+7]

Status: Recruiting

Identification of Vocal Biomarkers to Monitor the Health of People With a Chronic Disease

The CoLive Voice research project aims to identify vocal biomarkers of severe conditions and frequent health symptoms. The project is based on digital technologies and statistical algorithms. This is an international anonymous survey where vocal recordings are collected simultaneously with large validated clinical and epidemiological data, in the context of various chronic diseases or frequent health symptoms in the general population.

Participants needed: 50,000
Trial details
Age: 15+Biological sex: AllType: ObservationalSponsor: Luxembourg Institute of HealthUpdated: Sep 15, 2026Locations: 1
Eligibility criteria

Adolescents and adults > 15 years [+2]

Children < 15 years

Status: Recruiting

Observational Pharmaco-Epidemiology Research & Analysis

Greater advances are needed in two separate but related areas in healthcare: 1) the Clinical Decision Support Systems that complement the EHR use in support of routine patient care, population management and disease management; and 2) the use of the point-of-care observational data from the provider-patient encounter that support realworld medical research and healthcare quality measure assessment. Real-world evaluations of treatments of chronic diseases in the context of comorbid conditions and special populations (minorities, women, mentally ill, and those with addiction) are limited. The purpose of the OPERA database is to help address this unmet need in clinical research.

Participants needed: 2,000,000
Trial details
Age: 0+Biological sex: AllType: ObservationalSponsor: EpividianUpdated: Sep 11, 2026Locations: 1
Eligibility criteria

Patients who are treated in the practices who enroll and participate in the stud... [+1]

Patients who opt out of OPERA

Status: Recruiting

Susceptibility to Infectious Diseases in Obesity

The role of intestinal microbiota is becoming ever more important in the context of obesity, type II diabetes (T2D), and infectious disorders as represented by the emerging discipline "therapeutic microbiology". The gut microbiota is strictly interconnected with obesity and T2D playing also an important role in immune system regulation. Obesity and diabetes can lead to chronic inflammation, which results in the secretion of pro-inflammatory cytokines like IL-6, IL-1, and TNF-alpha, causing immune system alteration which predisposes patients with obesity and T2D to chronic infections. Therefore, the principal aim of the study is to investigate changes in gut microbiota composition between patients with chronic infections or not, so as to attribute to specific phyla the formation of the infections in these patients.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Azienda Ospedaliero Universitaria Maggiore della CaritaUpdated: Sep 10, 2026Locations: 1
Eligibility criteria

age between 18-65 years [+5]

psychological conditions that reduced the ability the comprehension of the study... [+11]

Status: Not yet recruiting

Alaska Alliance for Community Engagement Phase II: Partnership for Action Toward Health

The AK ACE-PATH Phase II study aims to pilot and implement a novel intervention, Tools for Arctic Health Promotion (TAHP), to address Alaska Native (AN) community priorities related to local health and community-level resilience.

Participants needed: 360
Trial details
Phase: Phase 1Age: 12+Biological sex: AllType: InterventionalSponsor: University of Alaska FairbanksUpdated: Sep 3, 2026Locations: 1
Eligibility criteria

Self-identify as a permanent resident of the study community [+2]

Does not have permanent residence in the community or has lived in the community... [+1]

Status: Recruiting

Improving Health and Wellness for People With Serious Mental Illness in Puerto Rico

This study evaluates the effectiveness of a culturally tailored intervention, Bridges to Better Health and Wellness (BRIDGES), aimed at reducing chronic disease disparities among Puerto Ricans with serious mental illness (SMI). Participants receive monthly sessions with health care managers to address patient-provider stigma and care coordination.

Participants needed: 300
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: Ponce Medical School Foundation, Inc.Updated: Aug 25, 2026Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

Families Implementing Good Health Traditions for Life

This study will provide evidence for the utility of using a community-engaged research approach to implement a tailored, family-oriented adaptation of the Diabetes Prevention Program that will have positive effects on risk factors associated with type 2 diabetes morbidity and mortality among Black families in a Southwest Georgia community.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Morehouse School of MedicineUpdated: Aug 5, 2026Locations: 1
Eligibility criteria

Family 1.a.) Black Parent/Guardian: age 18 years or older residing in the same h... [+3]

Individuals with severe psychological disorders that may prevent/interfere with... [+6]

Status: Recruiting

Impact of a Mobile Application-Based Medication Reminder on Treatment Adherence Among Patients With Chronic Diseases and Memory Impairment: A Nursing Leadership Perspective

This study aims to evaluate the impact of using a mobile application-based medication reminder on medication adherence among patients diagnosed with chronic diseases and memory impairment. Adherence to prescribed therapy is a significant challenge for this patient population, often leading to poor health outcomes and increased healthcare costs. From a nursing leadership perspective, innovative digital solutions can play a crucial role in supporting patient self-management. Using a quasi-experimental design, the study will investigate whether a customized mobile reminder system can effectively improve adherence rates and support patients in managing their therapeutic regimens.

Participants needed: 193
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mansoura UniversityUpdated: Jul 21, 2026Locations: 2
Eligibility criteria

Patients diagnosed with one or more chronic diseases requiring regular long-term... [+4]

Patients with severe cognitive impairment or advanced dementia who cannot intera... [+2]

Status: Not yet recruiting

Interactive Nature-Based Virtual Reality to Reduce Anxiety, Low Mood, and Feelings of Helplessness in Hospitalized Older Adults With Chronic Illness (Zenctuary VR+)

Prolonged hospitalization can reduce opportunities for independent activity, choice, and control and may contribute to passivity, low mood, anxiety, and distress in some older adults. Zenctuary VR+ is a seated, nature-based virtual reality program that combines calming environments with simple, low-demand activities. The active program allows participants to make choices, move between predefined locations, and influence elements of the virtual environment. Trained staff supervise every session and provide support when needed. The trial evaluates whether the interactive version of Zenctuary VR+ reduces psychological distress more than passive exposure to the same virtual environments. A total of 100 hospitalized adults aged 60 years or older will be randomly assigned to the interactive VR condition or the passive VR condition. Eligible participants are expected to remain hospitalized for at least four weeks following enrolment. Both groups will receive six sessions over three weeks. Psychological distress and related psychological factors will be assessed before the first session, immediately after the three-week intervention period, and four weeks after the final session.

Participants needed: 100
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Moholy-Nagy University of Art and DesignUpdated: Jul 21, 2026Locations: 3
Eligibility criteria

Aged 60 years or older [+6]

Cognitive impairment, defined as a score below 18 on the Montreal Cognitive Asse... [+7]

Status: Not yet recruiting

Therapeutic Drug Monitoring-baSed adalimuMab De-escalatiOn in nOn-infecTious cHronic Uveitis

Uveitis and its complications are thought to account for 10 to 15% of preventable blindness in Western countries. The diagnosis of chronic non-infectious uveitis (CNUI) can be made after exclusion of pseudo uveitis or infectious uveitis, in the case of any persistent uveitis or uveitis with frequent relapses occurring less than 3 months after cessation of treatment. Adalimumab (ADA), an anti-TNFα monoclonal antibody, has marketing authorization and is widely used in the treatment of UCNI as a relay to corticosteroids. The use of ADA has been optimized, in particular through Therapeutic Drug Monitoring (TDM), based on the determination of serum ADA levels and anti-ADA antibodies. Recently, an article showed that a strategy of spacing ADA administrations in RA patients with concentrations \>8 μg/mL was not inferior to standard.

Participants needed: 320
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire de Saint EtienneUpdated: Jul 10, 2026Locations: 11
Eligibility criteria

Informed and having signed the study consent form [+5]

Inability or refusal to understand and/or sign the informed consent form to part... [+4]

Status: Recruiting

Housing, Environment, And Living Conditions for Transformed Health

This project will compare the health effects of public housing renovation, neighborhood built and social environment improvements, and indoor air purification, alone and in combination, as well as the cost effectiveness of each approach. STUDY 1: The study will assess the effects of public housing and neighborhood environment (built and social) improvements on health-related behaviors, psychosocial and physiologic stress, and self-reported and physiological markers of lung health and chronic disease. STUDY 2: The study will determine whether indoor air purification can positively impact lung health in public housing sites not undergoing housing renovation, comparing a site near industrial pollution vs one less contaminated.

Participants needed: 460
Trial details
Age: 18-89Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Jul 6, 2026Locations: 1
Eligibility criteria

Adults age 18 years and older [+2]

Individuals who are not 18 years or older [+2]

Status: Recruiting

Improving Patients' Adherence to Their Chronic Treatments by Implementing a Simple, Standardized and Redundant Message Delivered by Healthcare Professionals.

The primary objective in this study is to achieve a 15% 6-month improvement in therapeutic adherence among patients with chronic pathologies, thanks to a simple, standardized and redundant message delivered by healthcare professionals during consultations/interviews Trained healthcare professionals deliver a simple, standardized and redundant 3-point message to patients, based on the levers of action concerning therapeutic adherence. This message is delivered with the aim of modifying the patient's behavior with regard to treatment intake.

Participants needed: 1,210
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Jul 1, 2026Locations: 10
Eligibility criteria

Adult patients (age ≥ 18 years) [+3]

Patients included in the control period. [+3]

Status: Not yet recruiting

Burden of Care and Health Literacy of Caregivers in the Emergency Department

This study aims to investigate the relationship between caregiver burden and health literacy among primary caregivers of patients with chronic diseases presenting to the emergency department. The study will be conducted in the Emergency Department of Yalova Training and Research Hospital and will include at least 300 caregivers. Data will be collected using a sociodemographic questionnaire, the Turkish Health Literacy Scale-32 (THLS-32), and the Zarit Burden Interview (ZBI). The findings are expected to contribute to a better understanding of caregivers' needs and to clarify the role of health literacy in caregiver burden among those providing care for individuals with chronic illnesses.

Participants needed: 350
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of YalovaUpdated: Jun 24, 2026
Eligibility criteria

Not listed

Status: Recruiting

Training Community Members to be Coaches to Deliver the HealthyLifetime Program

The goal of this randomized controlled study is to learn if, in addition to nurses, community members can be trained as health coaches to deliver the HealthyLifetime (HL) program to people without complex chronic health conditions, an intervention that provides a short-term and effective health coaching intervention delivered through a virtual platform to improve health, resiliency, and independent self-care to participants who are without complex chronic conditions. The main question it aims to answer is: • Can Community Health Coaches achieve the same level of competency and outcome as Nurse Health Coaches in participants without complex chronic conditions?

Participants needed: 300
Trial details
Age: 30+Biological sex: AllType: InterventionalSponsor: University of MichiganUpdated: Jun 22, 2026Locations: 2
Eligibility criteria

Be at least 30 years of age, with no more than three, uncomplicated chronic cond... [+9]

● Are less than 30 years of age. [+10]

Status: Recruiting

Impact of an Intervention Integrating the MPHS Nursing Model of Care on the Partnership in Health, With the Patient Followed in Primary Care by an Advanced Practice Nurse (APN) for One or More Stabilized Chronic Pathologies

The WHO and our governance advocate that health professionals should organize care around the patient, considering his or her values, needs and preferences, and enabling the patient to develop the capacity to self-manage the chronic health problems he or she faces. Chronic disease is an ongoing dynamic process and adaptation to this process is complicated by the interaction of several determinants: self-management capacity, level of health literacy, quality of life and experience of care. To best support chronic disease, the recommendation is to adopt a management strategy that allows chronic patients to play an active role in the management of their condition and in the day-to-day decision-making process. The management of chronic pathologies is one of the specialties in which Advanced Practice Nurses are positioned, in primary care, outside hospital. Nursing care benefits from care models that allow for more adapted responses, regarding particular care situations, or certain patient typologies. The Humanistic Partnership Health Care Model (MPHS) implement in current Advanced Practice Nurse (APN) practice.

Participants needed: 420
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire de Saint EtienneUpdated: Jun 10, 2026Locations: 5
Eligibility criteria

A patient receiving care from an advanced practice nurse (APN) for the managemen... [+2]

Status: Recruiting

Development and Evaluation of an Online Shared Decision-Making Educational Program for Nurses and Patients With Chronic Diseases

This study aims to develop and evaluate an online shared decision-making (SDM) educational program for nurses and patients with chronic diseases. Shared decision-making is a process in which healthcare professionals and patients make health-related decisions together based on the best available evidence and the patient's values and preferences. The study includes an evaluation phase. In the evaluation phase, the program will be tested among nurses working in general hospitals and adults with chronic diseases living in the community. Outcomes related to shared decision-making will be assessed at baseline, immediately after the 4-week program, and 1 month later. The study is expected to improve shared decision-making competence, experience, and preparedness among both nurses and patients.

Participants needed: 288
Trial details
Age: 19+Biological sex: AllType: InterventionalSponsor: Chungnam National UniversityUpdated: May 26, 2026Locations: 1
Eligibility criteria

Registered nurses currently providing direct patient care in participating gener... [+2]

Not currently engaged in direct patient care [+9]

Status: Not yet recruiting

Phenotype-Guided Weaning in Mechanically Ventilated Patients With Chronic Comorbidities

The goal of this clinical trial is to learn whether a phenotype-guided weaning strategy can help adults with chronic comorbidities be liberated from invasive mechanical ventilation earlier. It will also learn about the safety of this strategy. The main questions it aims to answer are: * Does the phenotype-guided weaning strategy increase the number of ventilator-free days within 28 days after enrollment? * Does the strategy improve the process and success of ventilator liberation? * What safety events occur when this strategy is used? Researchers will compare the phenotype-guided weaning strategy with standard care in mechanically ventilated patients with chronic cardiovascular, cerebrovascular, or respiratory comorbidities. In the intervention period, participants will receive a protocolized ventilator weaning pathway. This pathway includes assisted ventilation transition, daily weaning readiness screening, a 0 cmH2O continuous positive airway pressure test, spontaneous breathing trial, extubation assessment, and post-extubation respiratory support when appropriate. The phenotype-guided part of the strategy is mainly used for participants who fail a spontaneous breathing trial or have difficult weaning. These participants will undergo structured ABCDE screening to identify the main phenotype or mechanism of weaning failure: * A: airway or lung dysfunction * B: brain dysfunction, including delirium, anxiety, agitation, or impaired consciousness * C: cardiac dysfunction * D: diaphragm or respiratory muscle dysfunction * E: endocrine, metabolic, or nutritional problems Based on the identified phenotype, clinicians will provide targeted assessment and treatment. Participants will be followed for ventilator-free days through day 28 and for clinical outcomes through day 90.

Participants needed: 1,380
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Southeast University, ChinaUpdated: May 19, 2026
Eligibility criteria

Age 18 years or older. [+4]

Severe neuromuscular disease, such as Guillain-Barre syndrome, myasthenia gravis... [+5]

Status: Recruiting

Click & Pick Study

Unhealthy diets significantly contribute to major preventable chronic diseases including type 2 diabetes, obesity, heart disease and stroke, which disproportionally impact racial/ethnic minority groups and those with lower income \[1-3\]. Although taxes and warning labels targeting sugar-sweetened beverages (SSB) have been successful at shifting behavior \[4-7\], there are many other ultra-processed food products that contribute to unhealthy diets \[8\]. What is less well-known is whether a suite of healthy food policies that are expanded to target a range of ultra-processed foods can shift dietary choices and intake in meaningful ways. Our research team's long-term goal is to identify and understand the degree to which combinations of healthy food policies can improve nutrition security and reduce nutrition-related diseases.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of PennsylvaniaUpdated: May 18, 2026Locations: 1
Eligibility criteria

≥18 years old [+9]

Does not meet all of the inclusion criteria [+3]

Status: Recruiting

Whole-life Investigation of Lishui Longevity

1. To establish a standardized, normalized and scientific joint screening and follow-up management system for chronic disease multimorbidity in Lishui City, and early identify common risk factors of major chronic diseases such as cardiovascular and cerebrovascular diseases and tumors. 2. To carry out targeted intervention and long-term follow-up for high-risk populations, reduce the incidence risk of major chronic diseases in the target population, improve residents' health status and grassroots comprehensive prevention and treatment capacity of chronic diseases, and provide scientific evidence and practical support for the construction of Healthy Lishui.

Participants needed: 4,500
Trial details
Age: 30-80Biological sex: AllType: ObservationalSponsor: The Fifth Affiliated Hospital of Wenzhou Medical University & Lishui Central HospitalUpdated: May 18, 2026Locations: 1Duration: 10 Years
Eligibility criteria

Aged 30 to 80 years old; male-to-female ratio of 1:1; permanent residents in Lis...

Individuals ever diagnosed with malignant tumors or cardiovascular and cerebrova...

Status: Not yet recruiting

Moxie Self-Management and Education Support Program

Health education and self-management support are key facilitators of health behaviours. Moxie is a mixed media, self-management, education and support program for Albertans living with cardiovascular-related chronic conditions. Moxie is built upon our previous work within the ACCESS study (2015-21, n=4761), a RCT that previously tested the Moxie intervention in Alberta. Results demonstrated that MOXIE reduced the rate of hospitalizations (notably for hypertension, angina, hyper/hypoglycemia, heart failure decompensation, and acute kidney complications) by 34% in a population of low-income seniors living with cardiovascular-related chronic conditions. However, before Moxie can be effectively implemented province-wide, another trial is necessary to determine whether benefits can be observed in a larger cohort of patients with cardiovascular-related chronic conditions recruited immediately after hospital discharge (n=9000). Furthermore, the effectiveness of the two components of the ACCESS trial intervention will be assessed individually: (a) The Moxie Program, a tailored health and disease education component developed by a user-experience-centric design process incorporating patients, behavioural scientists, disease specialists, health system administrators and marketing/advertising professionals; and (b) the facilitated relay of clinical information to healthcare providers (letters). The trial is designed as a 2x2 factorial pragmatic, individual-level randomized pragmatic trial of these different interventions. This would yield the following groups: 1. Moxie SMES Program 2. Facilitated Relay 3. Moxie SMES Program and Facilitated Relay 4. True control Self-management education and support (SMES) intervention: This includes weekly physical mailers sent directly to patients' homes throughout the study containing information about chronic conditions, medication use, diet, physical activity, smoking cessation, and self-management/wellness principles. These messages will be refined by the social impact creative design partner and reviewed by clinicians and patients to ensure clinical safety and appropriate tone. Weekly mailers will encourage participants to enroll and consent to participate in the digital program by scanning a QR code or accessing a website where they will sign up for their own personalized Moxie mobile health app, complete a digital consent form and opt-in for electronic delivery of Moxie messages. Facilitated relay intervention: Participants allocated to this intervention will receive letters by mail, one addressed to them, one to their primary care provider, and one to their pharmacist. The letters will not be sent to their primary care provider directly; rather, they will be sent to patients who will be encouraged to take them to their primary care provider and pharmacist should they decide to do so. We hope this will empower patients to start discussions with their healthcare providers. This also supports patient autonomy by enabling patients to decide whether they want to take them to their provider or not. If for whatever reason they do not feel that this is going to be beneficial or of interest, they are not required to do so. The letter would contain a note to the patient's healthcare provider stating that their patient is at-risk of cardiovascular disease and that evidence has shown that the pharmacotherapy is effective in improving outcomes for patients similar to the participant. The primary outcome is readmission for cardiovascular-specific ambulatory care-sensitive conditions (ACSC) based on the most responsible diagnosis listed in CIHI Discharge Abstract Database-(DAD), using established algorithms within 12 months from randomization. This outcome includes all repeat admissions in the study period as recorded in the health record. This outcome is a count variable. We will calculate and compare each intervention arm's mean number and distribution of hospitalizations.

Participants needed: 9,000
Trial details
Age: 40-85Biological sex: AllType: InterventionalSponsor: University of CalgaryUpdated: May 11, 2026
Eligibility criteria

Not listed

Status: Recruiting

Psychosocial, Environmental, and Chronic Disease Trends in Puerto Rico

The overall goal is to identify trends and longitudinal associations in psychosocial, food-related, and cardiometabolic risk factors that can guide public health priorities and future research needs aimed at reducing cardiovascular-related disparities in Puerto Rico. To this end, investigators will establish 'PROSPECT: Puerto Rico Observational Study of Psychosocial, Environmental, and Chronic disease Trends', an island-wide, longitudinal population cohort of 2,500 adults (30-75 years) in PR recruited with a community-wide sampling strategy, and assessed in a network of several partner clinics across the island. The study will collect comprehensive data on multiple psychosocial, dietary, and food-related factors, CVD biological markers, and medical record data, with follow-up at 2-years, and will assess variations by urban-rural area and by timing before-after Maria.

Participants needed: 2,500
Trial details
Age: 30-75Biological sex: AllType: ObservationalSponsor: Harvard School of Public Health (HSPH)Updated: May 5, 2026Locations: 1
Eligibility criteria

Age 30-75 years old at the time of enrollment [+4]