- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07497841
Development and Validation of a KAP Questionnaire for Secondary Hypertension: Evaluating a Community Short-Video Intervention in Rural Beijing (KAP-SHORT)
Development and Application of a KAP Questionnaire for Secondary Hypertension: Evaluating a Community-Targeted Short-Video Intervention in Suburban Beijing
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a two-phase, non-randomized, community-based clinical trial carried out in 8 communities in Miyun District, Beijing.
Phase 1: Scale Development and Validation We develop and validate an 18-item Knowledge, Attitudes, and Practices (KAP) scale specifically for secondary hypertension in community residents. Psychometric properties including reliability, internal consistency, and validity are tested using item analysis, exploratory factor analysis, and confirmatory factor analysis.
Phase 2: Intervention Evaluation We enroll hypertensive patients and their family members. All participants receive a 1-week, community-centered targeted short-video intervention delivered through community WeChat groups by trained local physicians. The intervention includes five 1-minute standardized educational videos covering core topics: definition, etiology, clinical manifestations, high-risk groups, and screening methods for secondary hypertension.
Outcomes and Assessments The secondary hypertension KAP scale is administered at baseline (before intervention) and within 24 hours after intervention to measure changes in knowledge, attitudes, and practices. Video engagement (view count, completion rate, viewing duration) is automatically recorded. We compare pre- and post-intervention scores and identify subgroups with greater improvement, including rural residents, those with lower educational attainment, older adults, and patients with hypertension.
The study aims to provide a valid assessment tool and a scalable, community-based health education model to improve secondary hypertension-related awareness and behaviors, especially for rural and low-educated populations.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Beijing, China
- Peking University First Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Permanent residents aged ≥18 years with basic comprehension abilities, capable of completing the online questionnaire independently or with assistance
- Voluntary participation and signed informed consent
For Phase 2 (Intervention Phase) only:
- Individuals with confirmed hypertension or family members cohabiting with hypertensive patients
- Member of a community WeChat group with the ability to receive and view short videos, and to complete online questionnaires independently or with assistance
Exclusion Criteria:
- - Cognitive impairment that would interfere with understanding the questionnaire or video content
- Prior participation in standardized secondary hypertension public education programs
- Inability to use WeChat or access short videos (for Phase 2)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Community-Based Short-Video Intervention Group
Participants received a one-week short-video intervention on secondary hypertension.
Five one-minute videos covered definition, symptoms, screening, treatment, and prognosis.
Videos were delivered via community WeChat groups.
Community physicians monitored engagement.
KAP scores were measured pre- and post-intervention.
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Participants received five one-minute educational videos about secondary hypertension via community WeChat groups over one week.
Videos covered definition, symptoms, screening, treatment, and prognosis.
Content was reviewed by specialists.
Community physicians monitored engagement and sent reminders.
The intervention aims to improve KAP levels.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in total score of the Secondary Hypertension Knowledge, Attitudes, and Practices (KAP) scale
Time Frame: Baseline (1 day before intervention) and within 24 hours after the 1-week intervention
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The total score of the validated 18-item KAP scale for secondary hypertension will be measured at baseline and post-intervention.
The scale includes knowledge, attitudes, and practices dimensions using a 5-point Likert scale.
A higher total score indicates better knowledge, more positive attitudes, and better practices related to secondary hypertension.
The primary outcome is the mean change from baseline to post-intervention.
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Baseline (1 day before intervention) and within 24 hours after the 1-week intervention
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- PKUFH-JFXGXY
- 202501 (National Health Education Center Research Grant)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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