Development & Preliminary Validation of a Community Health Education Program

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine

About this trial

This study analyzes the needs of patients regarding the content and form of home-based health education through interviews, and constructs a health education program tailored to these needs. A practical WeChat mini-program is developed to enable patients with interstitial lung disease to promptly access comprehensive health education information, consult about follow-up visits, and check test reports during their home care period, ultimately aiming to improve patients' quality of life and reduce medical consumption.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Complicated with other life-threatening diseases; Consciousness disturbance or mental illness; Currently participating in other clinical trials that may affect this study.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • The use and guidance of the mini-program

    Behavioral

    Interventions were conducted through routine health education, telephone follow-ups, and questionnaire surveys during reconsultations. Health education covered disease knowledge, medication guidance, rehabilitation guidance, dietary guidance, and psychological guidance. After discharge, patients were followed up by telephone or home visit once a month, and questionnaire data were collected during their reconsultations. The use of a mini-program was added with corresponding guidance: patients were instructed to proficiently use the mini-program's functions for accessing health education information, interacting with medical staff, and noting key points for questionnaire completion, and were advised to fill out the questionnaire monthly. Doctors and nurses were guided to skillfully use the mini-program to push health education-related knowledge to patients at irregular intervals, and medical staff were trained on the effective collection of questionnaire data and data statistics.

Treatment groups

92 Participants
are divided into 2 treatment groups
Group A: Control Group0 interventions
Group B: Experimental Group1 intervention

Trial outcomes

Primary outcomes

1

Improve patients' quality of life and reduce medical consumption

Guide doctors and nurses to proficiently use the mini-program to push health education-related knowledge to patients at irregular intervals, and instruct medical staff on the effective collection of questionnaire data and data statistics.

Time frame
One year after the start of recruitment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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