Psychosocial, Environmental, and Chronic Disease Trends in Puerto Rico (PROSPECT)

  • STATUS
    Recruiting
  • End date
    Dec 31, 2023
  • participants needed
    2000
  • sponsor
    Harvard School of Public Health (HSPH)
Updated on 25 March 2022
chronic disease
Accepts healthy volunteers

Summary

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 2,000 adults (30-75 years) in PR recruited with a multi-frame sampling of probabilistic plus community approaches, 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.

Details
Condition Heart Diseases, Type2 Diabetes, Hypertension, Obesity, Dyslipidemias, Metabolic Syndrome, Cardiovascular Diseases, Chronic Disease, Inflammation, Psychological Stress, Physiological Stress, Depressive Symptoms, Coping Behavior, Diet Habit, Lifestyle
Clinical Study IdentifierNCT03794531
SponsorHarvard School of Public Health (HSPH)
Last Modified on25 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 30-75 years old at the time of enrollment
Non-institutionalized
Living in PR at the time of the first interview and the year before and not planning to move from the island within 3 years
Able to answer questions without assistance
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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