Skip to main content
OpenTrials
Completed

NCT Number: NCT05792618

Stroke Patients and Family Longitudinal Study in Rural China

SaFaRI is a large prospective cohort study in Hebei Province, rural Northern China including 1,299 stroke patients and their spouses. Follow-up visits take place from baseline until the fifth year after the baseline survey, investigating the lifestyle and health behavior, disease history, medication and adherence to medication, health status and self-reported health, cognitive function, and medication cost. As additional measures, the investigators will collect information on hospitalization, recurrence, and vital status from county medical insurance system and death record system. Patients will also have a physical examination comprising of assessment of blood pressure, weight, height, waist circumference, neck circumference, grip strength and the "Timed Up and Go" test.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Nanhe County

Xingtai, Hebei, 054400, China

About this study

SaFaRI is a prospective longitudinal follow-up study based on a cluster-randomized controlled trial (System-integrated technology-enabled model of care to improve the health of stroke patients in rural China, SINEMA study) to evaluate the effectiveness of the SINEMA model to improve the secondary prevention of stroke in Nanhe County, a rural area of Hebei Province, China. A total of 1299 stroke patients were included at baseline, of which 25 villages received the SINEMA intervention package.

TThe SaFaRI study conducted a new follow-up round for participants of the SINEMA trial in 2023. Initially including 1299 stroke patients at baseline, this follow-up also encompassed the patients' spouses. The study aimed to: 1) Evaluate the stroke patients' blood pressure reduction, adherence to secondary prevention medications, physical activity, recurrence of stroke, hospitalization rates, and mortality. 2) Assess the long-term effectiveness of the SINEMA intervention model after a 5-year follow-up by examining the knowledge, attitudes, and practices of village doctors. 3) Establish a dynamic and continuous cohort of stroke patients, representative of northern rural China, using data from the baseline and the 1-year follow-up visits.

In 2024, the cohort underwent another follow-up, which expanded to include the collection of additional diseases and their diagnosis dates, and also surveyed patients regarding their sensory and viatality function.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

The eligible stroke patients should meet all the following criteria: those who

  • aged more than 18 years old
  • have a history of stroke diagnosed at county or higher-level hospitals, and are in stable condition;
  • have at least a basic communication ability;
  • give their informed consent and are willing to participate in the study.
  • have participated in the primary care-based integrated mobile health intervention for stroke management in rural China (SINEMA).

And excluding those who

  • have serious mental diseases;
  • have other serious diseases, and have a remaining life expectancy of less than 6 months.

The eligible spouses should meet all the following criteria: those who

  • aged more than 18 years old
  • is the spouse of the stroke patient who participates in SINEMA study;
  • have at least a basic communication ability;
  • give their informed consent and are willing to participate in the study.

And excluding those who

  • have serious mental diseases;
  • have other serious diseases, and have a remaining life expectancy of less than 6 months.

Treatment and study plan

Primary outcomes

  1. Blood pressure

    Time frame: change from baseline to follow-up

    change in blood pressure

  2. Weight

    Time frame: change from baseline to follow-up

    change in weight

  3. Height

    Time frame: change from baseline to follow-up

    change in height

  4. Grip strength

    Time frame: at various follow-up stages

    Grip strength (kilogram) will be estimated through the dynamometer (YuejianTM WL-1000, Nantong, China). Trained examiners will instruct people to hold the dynamometer and squeeze the handle for a few seconds. This study both measures right and left-hand grip strength twice in each hand. The grip strength will be recorded separately. If the average grip strength of both right and left hand of is all less than the criteria (man < 30 kg, woman < 20 kg), it is defined as weak grip strength.

  5. Neck circumference

    Time frame: at various follow-up stages

    participants' neck circumference

  6. Waist circumference

    Time frame: at various follow-up stages

    Participants' waist circumference

  7. Mobility

    Time frame: at various follow-up stages

    measured by timed-up-and-go test, a simple and quick functional mobility test that requires the participants to stand up, walk 3 meters, turn, walk back, and sit down

Secondary outcomes

  1. Cognitive function

    Time frame: at various follow-up stages

    measured by a brief version of the Community Screening Instrument for Dementia (CSI-D). The brief CSI-D was developed by Martin Prince, which consist of 7 cognitive items (Prince, M., Acosta, D., Ferri, C. P., Guerra, M., Huang, Y., Jacob, K. S., ... & 10/66 Dementia Group. (2011). A brief dementia screener suitable for use by non-specialists in resource poor settings-the cross-cultural derivation and validation of the brief Community Screening Instrument for Dementia. International journal of geriatric psychiatry, 26(9), 899-907.). The score of the brief CSI-D ranges from 0 to 9, with 0-4 represent Probable dementia, 5-6 represent Possible dementia, and 7-9 represent Normal.

  2. Mental Health

    Time frame: change from baseline to follow-up

    measured by using Patient Health Questions-9, an international standard instrument for screening, monitoring and measuring the severity of depression. The total scores range from 0 (no depression) to 27 (severe depression).

  3. Health related quality of life

    Time frame: change from baseline to follow-up

    measured using EuroQol-5 Dimensions-5L (EQ5D-5L). EQ-5D-5L descriptive system comprises the following five dimensions, each describing a different aspect of health: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. For each domain, the total scores range from 0 (indicating no problem) to 5 (indicating unable to/extreme problems). In addition, the participants were required to assess how their health is today by write a number from 0 to 100 on the numbered scale. 100 means the best health the participant can image, 0 means the worst health the participant can image.

  4. Medication adherence

    Time frame: change from baseline to follow-up

    measured using 4 item Morisky Green Levine Scale-4 (MMAS-4), which scores adherence from 0-4 and continuation of medication taking is measured by the total months of medication taking

  5. Disease history

    Time frame: change from baseline to follow-up

    collected through questionnaire and medical insurance records

  6. Lifestyle risk factors

    Time frame: change from baseline to follow-up

    The factors include lack of exercise, alcohol, diet, obesity, and smoking, and will be collected through questionnaire.

  7. Basic activities of daily living

    Time frame: at various follow-up stages

    measured by the basic activities of daily living (ADL). The basic ADL include the following categories: Ambulating, Feeding, Dressing, Personal hygiene, Continence, and Toileting. The ADL score ranges from 0 to 12. Limitation in ADL was defined as being scored greater than 0 on ADL scales, i.e., having some or severe limitation in at least one ADL item. Higher scores mean a worse functional independence.

  8. Instrumental activities of daily living

    Time frame: at various follow-up stages

    measured by the Lawton Instrumental Activities of Daily Living (IADL) Scale to evaluate independent living skills. The scale measures eight domains of function, including food preparation, housekeeping, laundering. The IADL score ranges from 0 to 14. Limitation in IADL was defined as being scored greater than 0 on IADL scales, i.e., having some or severe limitation in at least one IADL item. Higher scores mean a worse functional independence.

  9. Disability

    Time frame: change from baseline to follow-up

    measured using modified Rankin Scale (ranged 0 (no symptom) to 5 severe disability)

  10. Multimorbidity

    Time frame: at various follow-up stages

    Assessed by determining whether participants had additional diseases diagnosed in the hospital, excluding stroke

  11. Sensory and vitality functions

    Time frame: at various follow-up stages

    Assessed by querying your usual use of corrective lenses for vision, your ability to recognize distant and close objects, your use of hearing aids, and the quality of your hearing in different conditions.

Sponsors and collaborators

Lead sponsor

Duke Kunshan University

Other

Collaborators

  • Peking Union Medical College

Registry information

Official study title

Stroke Patients and Family in Rural China: A Longitudinal Study in Hebei Province

Acronym: SaFaRI

Important dates

Study start
2022
Primary completion
2023
Study completion
2024
First posted
Mar 31, 2023
Registry last updated
Jun 10, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.