Development and Validation of a KAP Questionnaire for Secondary Hypertension: Evaluating a Community Short-Video Intervention in Rural Beijing (KAP-SHORT)

March 23, 2026 updated by: Peking University First Hospital

Development and Application of a KAP Questionnaire for Secondary Hypertension: Evaluating a Community-Targeted Short-Video Intervention in Suburban Beijing

This is a two-phase, non-randomized clinical trial conducted in eight communities in Miyun District, Beijing. The study first develops and validates a reliable 18-item questionnaire (Knowledge, Attitudes, and Practices [KAP] scale) to assess community residents' understanding, attitudes, and behaviors related to secondary hypertension. Then, we evaluate whether a 1-week community-centered short-video health education intervention (five 1-minute videos delivered via community WeChat groups by local physicians) can improve residents' secondary hypertension-related knowledge, attitudes, and practices. We will compare scores before and after the intervention, and analyze which groups (such as rural residents, people with lower education, older adults) benefit more. This study aims to provide a simple assessment tool and a scalable health education model for secondary hypertension in community settings, especially for rural and low-educated populations.

Study Overview

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

Interventional

Enrollment (Actual)

1062

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Beijing, China
        • Peking University First Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
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.

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
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.
Baseline (1 day before intervention) and within 24 hours after the 1-week intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2025

Primary Completion (Actual)

January 31, 2026

Study Completion (Actual)

March 1, 2026

Study Registration Dates

First Submitted

March 9, 2026

First Submitted That Met QC Criteria

March 23, 2026

First Posted (Actual)

March 27, 2026

Study Record Updates

Last Update Posted (Actual)

March 27, 2026

Last Update Submitted That Met QC Criteria

March 23, 2026

Last Verified

March 1, 2026

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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