Approval Date
2015.3.14
– (Ph.D) – Epidemiologist – Modeling in Health Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran – aliahmadi2007@gmail.com
Approval date
2015.3.14
The study was conducted in accordance with the guidelines of the Declaration of Helsinki and the National Ethical Guidelines in Biomedical Research in Iran. The study was approved by the Ethics Committee of the Shahrekord University of Medical Sciences (SKUMS) (IR.SKUMS.REC.1394.286) at regional and national scales in 2014.
Starting date
November 2015
the pre-pilot phase of the study from 22 Nov 2015 to 10 Sept 2016.
Goals
The aims of the Shahrekord PERSIAN Cohort Study (SPCS) are: i) to evaluate the prevalence and long-term trends of NCDs and their outcomes in an Iranian province with unique geographical, ethnic, and socioeconomic characteristics, ii) to investigate associations of environmental and genetic/ethnic factors with the prevalence and incidence of NCDs and their outcomes, iii) to examine the interplay between genetic/ethnic and environmental factors in the etiology and prevention of NCDs, iv) to provide the basis for various types of epidemiological studies (e.g., social, spatial, molecular epidemiology) and generate scientific evidence that may contribute to improving public health in the Chaharmahal and Bakhtiari (CH&B) province, v) to provide a research and education platform and a resource for national and international collaboration and to make the research community aware of the existence of large cohorts around the world.
Study population
This population-based prospective cohort study recruited participants from the Chahrmahal & Bakhtiari province in Southwest Iran. A total of 10075 participants were recruited from the districts of Shahrekord and Ardal, situated in urban (7034 participants) and rural (3041 participants) areas, respectively.
Shahrekord cohort center included people between the ages of 35 and 75 (both sexes), living in ten urban areas in Shahrekord and ten rural areas in Ardal district.
Sampling method and sample size
The multistage sampling method (stratified proportional cluster sampling) was applied to recruit participants. N=10075
Data Collection
Questionnaires, checklist, observation, interview
Questionnaires and research tools used in the Shahrekord PERSIAN Cohort Study
Follow up Methods
Phone, Annual follow-ups (200,000 person-year) of the cohort were designed to be conducted up to 2036.
The follow-up process aimed to register new cases of common NCDs and their outcomes, including death, cause of death, hospital admissions, and update information on exposures. The SPCS focuses primarily on the most common NCDs, including cardiovascular diseases, cancers, and the main endocrine, digestive, hepatic, renal, psychiatric, and respiratory disorders, defined using the International Classification of Diseases 10th version (ICD-10). The annual follow-up of the SPCS began in October 2017 and included questionnaires, medical examinations, and linkage with other databases (death, cancer registry). The study follow-up is done annually through telephone calls and links with health databases to identify disease outcomes. More specifically, the follow-up of participants is performed in two forms: an active form including phone interviews and face-to-face interviews (when outcomes occur), and an inactive form, including self-reports.
Main Exposures
The study collected data on a large number of exposures such as demographics, general health, lifestyle, dietary habits, nutrition and eating habits, employment, social integration, quality of life (e.g., sleep patterns, stress), physical activity, anthropometric indexes, occupational history, living place, family medical history and use of medication, and the number of anthropometric and physiological measures (e.g., respiratory capacity tests, electrocardiograms).
A rich biobank was created by collecting, in all cohort participants, samples from whole blood, serum, plasma, buffy coat, hair, nail, and urine. Diseases were ascertained from clinical examinations, biochemical variables, interviews, and linkage with medical records registered in the integrated health information system.
Outcomes
Incidence of common NCDs (cardiovascular diseases, cancer, gastrointestinal, respiratory, renal, hepatic, accidents, injury and neurological diseases, MS), the trend of risk factors, hospitalization, disability, and death were considered the outcomes of the cohort.
‘Multimorbidity’ was defined as the co-existence of two or more chronic diseases in the cohort, and we further categorized participants into groups defined as having 0, 1, 2, or 3 and more comorbidities; the following common NCDs were considered: myocardial infarction, ischemic heart disease, hypertension, diabetes mellitus, hypo/hyperthyroidism, stroke, epilepsy, chronic headache, chronic kidney disease, arthritis, osteoporosis, chronic obstructive pulmonary diseases, fatty liver, cancers, asthma, gastrointestinal conditions, peptic ulcer, Crohn’s disease, ulcerative colitis, multiple sclerosis, chronic depression and psychological disorders).
Co-Investigators
Co-Investigators
Prospective cohort studies are considered ideal choices to study multiple outcomes and risk factors for Non-communicable diseases (NCDs).
Gallery
Data collection inestruments
The follow-up process aimed to register new cases of common NCDs and their outcomes, including death, cause of death, hospital admissions, and update information on exposures. The SPCS focuses primarily on the most common NCDs, including cardiovascular diseases, cancers, and the main endocrine, digestive, hepatic, renal, psychiatric, and respiratory disorders, defined using the International Classification of Diseases 10th version (ICD-10). The annual follow-up of the SPCS began in October 2017 and included questionnaires, medical examinations, and linkage with other databases (death, cancer registry). The study follow-up is done annually through telephone calls and links with health databases to identify disease outcomes. More specifically, the follow-up of participants is performed in two forms: an active form including phone interviews and face-to-face interviews (when outcomes occur), and an inactive form, including self-reports. Identification of outcomes is made through automatic notifications received from the healthcare system and linkage with other health databases such as the National Disease and Health Outcome Registry Systems.
Metadata Dictionary
SPCS Timeline
2015.3.14
November 22, 2015 to September 10, 2016
October 6, 2016 to December 20, 2016
Enrollment from: 7034 urban participants : 6 Oct 2016- 22 Aug 2018
Enrollment from: 3041 rural participants : 23 Aug 2018- 22 Aug 2019
Follow-up and outcomes ascertainment
Ongoing Follow-up
The second wave of the reassessment phase was started in September 2021.
Book: Setup experience, Report of Enrollment Phase and
Preliminary Results for Prospective Epidemiological Research Studies in IrAN, Shahrekord PERSIAN Cohort Study
Papers:
3- The protocol of a population-based prospective cohort study in southwest of Iran to analyze common non-communicable diseases: Shahrekord cohort study
6- Study of correlation between chronic stressor, biochemical markers and hematologic indices in Shahrekord Cohort Study: A population-based cross-sectional study
8- Quality of life and its related factors among participants in Shahrecord – Iran cohort study
11- Socioeconomic gradient in physical activity: findings from the PERSIAN cohort study
13- The PERSIAN Cohort: Providing the Evidence Needed for Healthcare Reform
27-Repositioning of the global epicentre of non-optimal cholesterol
28-