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CompletedNCT05792618SaFaRIUpdated Jun 10, 2024

Stroke Patients and Family Longitudinal Study in Rural China

An observational study in Stroke, sponsored by Duke Kunshan University. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-10.

Sponsored by Duke Kunshan University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,299
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Stroke

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03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 1,299 is above the median of 160 across 1,692 observational studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Duke Kunshan University is the lead sponsor of 11 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The participants will be recruited from the SENEMA study sample and their spouses. The SENEMA study sample has the following characteristics: over 18 years old, have a history of stroke diagnosed at county hospital or higher-level facilities, are currently in a clinically stable condition and not receiving acute stroke treatment, will live in this village for at least 9 months during the next 12 months, have basic communication ability and give their informed consent. A total of 1299 individuals were included at baseline. After excluding those who died during the 1-year follow-up (n = 30), a total of 1269 people will be included in the 5-year follow-up.

Eligibility criteria

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.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,299 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Blood pressure

    change in blood pressure

    Time frame: change from baseline to follow-up

  2. Weight

    change in weight

    Time frame: change from baseline to follow-up

  3. Height

    change in height

    Time frame: change from baseline to follow-up

  4. Grip strength

    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.

    Time frame: at various follow-up stages

  5. Neck circumference

    participants' neck circumference

    Time frame: at various follow-up stages

  6. Waist circumference

    Participants' waist circumference

    Time frame: at various follow-up stages

  7. Mobility

    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

    Time frame: at various follow-up stages

Secondary outcomes

  1. Cognitive function

    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.

    Time frame: at various follow-up stages

  2. Mental Health

    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).

    Time frame: change from baseline to follow-up

  3. Health related quality of life

    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.

    Time frame: change from baseline to follow-up

  4. Medication adherence

    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

    Time frame: change from baseline to follow-up

  5. Disease history

    collected through questionnaire and medical insurance records

    Time frame: change from baseline to follow-up

  6. Lifestyle risk factors

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

    Time frame: change from baseline to follow-up

  7. Basic activities of daily living

    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.

    Time frame: at various follow-up stages

  8. Instrumental activities of daily living

    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.

    Time frame: at various follow-up stages

  9. Disability

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

    Time frame: change from baseline to follow-up

  10. Multimorbidity

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

    Time frame: at various follow-up stages

  11. Sensory and vitality functions

    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.

    Time frame: at various follow-up stages

07

Study locations

1 site
  • Nanhe County
    Xingtai, Hebei 054400, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 10, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05792618
Lead sponsor
Duke Kunshan University
Collaborators
Peking Union Medical College
Responsible party
Sponsor
First posted
Mar 31, 2023
Start date
Sep 1, 2022
Primary completion
Jun 1, 2023
Completion
Jun 1, 2024
Last update
Jun 10, 2024

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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