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Recruiting NCT05691790

NCT05691790 Older People's Preventive Care Utilization

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Clinical Trial Summary
NCT ID NCT05691790
Status Recruiting
Phase
Sponsor The University of Hong Kong
Condition Health Communication
Study Type INTERVENTIONAL
Enrollment 270 participants
Start Date 2024-10-01
Primary Completion 2025-05-31

Trial Parameters

Condition Health Communication
Sponsor The University of Hong Kong
Study Type INTERVENTIONAL
Phase N/A
Enrollment 270
Sex ALL
Min Age 70 Years
Max Age N/A
Start Date 2024-10-01
Completion 2025-05-31
Interventions
MMA and patient activation intervention schemeControl Group

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Brief Summary

Objectives: To empower older people's decision making for taking the recommended vaccines including seasonal influenza vaccines, pneumococcal vaccines, and COVID-19 vaccine (if it is recommended annually). Hypotheses to be tested: The interventions designed using Mental Models Approach and Patient Activation Approach will promote older people's confidence in knowledge and skills regarding vaccination decisions, perceived self-efficacy in self-management of health, positive emotional engagement with vaccination decisions and a positive future time perspective which will subsequently promote their uptake of the recommended vaccines. Design and subjects: This will be a two-arm randomized control trial. Subjects will be community-dwelling older people aged 70 years or above. Instruments: A questionnaire will be used to collect baseline data before the interventions and follow-up data 1 months and 4 months, respectively, after the end of interventions. Interventions: Interventions included one booklet to communicate information about preventive care by bridging expert knowledge and older people's existing mental models, and six patient activation sections conducted over telephone. One patient activation section will be delivered per week by trained medical students. Main outcome measures: Main outcomes will be participants' uptake of the three recommended vaccines assessed at 1 month and 4 months after the end of interventions. Data analysis and expected results: Generalized estimating equation logistic regression will be used to assess the intervention effects. The investigators expect that the interventions can promote at least 20% increase in uptake of any one of the three recommended vaccines in the intervention group compared with the control group.

Eligibility Criteria

Inclusion Criteria: * Community-dwelling older persons aged 70 years who did not persistently receive seasonal influenza vaccine over the past three years (2020-2022) and/or have never received the pneumococcal vaccine (one dose of the 23-valent pneumococcal polysaccharide vaccine (23vPPV) or the 13-valent pneumococcal conjugate vaccine (PCV13)). * Being able to communicate with Cantonese, or Mandarin (the two main spoken language in Hong Kong) and being able to read Chinese. * Inclusion criteria for the informant include age above 18 and can understand Cantonese or Mandarin Exclusion Criteria: * having psychiatric disorders, dementia, or other cognitive difficulties which impede communication or understanding of the intervention and having functional disabilities which impede access to health care services. * subjects who had medical contraindications for immunization.

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