Actively Recruiting

Phase Not Applicable
Age: 70Years +
All Genders
Healthy Volunteers
ID05691790

Empowering Older People's Preventive Care Utilization Through Mental Model Approach and Patient Activation Approach: a Randomized Control Trial to Promote Vaccination Uptake

Led by The University of Hong Kong · Updated on 2025-03-30

270

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying ways to help older adults, aged 70 years and above, make informed decisions about receiving recommended vaccines, including seasonal influenza, pneumococcal, and possibly annual COVID-19 vaccines. The study aims to improve older people's confidence, self-efficacy, emotional engagement, and positive future outlook to increase vaccination uptake. This trial is a randomized controlled study focusing on community-dwelling older people and uses the Mental Models Approach and Patient Activation Approach to design interventions. The study compares two groups: an intervention group receiving a specially designed booklet and six weekly telephone sessions using motivational interviewing techniques to activate patient engagement, and a control group receiving a pamphlet with vaccine recommendations plus six short telephone calls offering general health advice. The booklet is crafted to address older adults' mental models and emotional decision-making preferences, while the telephone sessions aim to support knowledge, skills, and confidence in vaccination decisions. Participants will be involved in baseline questionnaires and follow-up assessments at one and four months after the interventions to track vaccination uptake and changes in attitudes, knowledge, emotions, and behaviors. Data will be collected through questionnaires and telephone interviews, and outcomes like vaccine uptake rates and patient activation measures will be analyzed. The study includes careful monitoring to ensure participant understanding and consent, with data handled securely and anonymously throughout the trial.

CONDITIONS

Brief Title

Older People's Preventive Care Utilization

Who Can Participate

Age: 70Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Community-dwelling older persons aged 70 years or above
  • Did not consistently receive seasonal influenza vaccine over the past three years (2020-2022) and/or have never received pneumococcal vaccine (23vPPV or PCV13)
  • Able to communicate in Cantonese or Mandarin and able to read Chinese
  • Informant aged above 18 years who can understand Cantonese or Mandarin
Not Eligible

You will not qualify if you...

  • Having psychiatric disorders, dementia, or cognitive difficulties that impede communication or understanding of the intervention
  • Having functional disabilities that impede access to health care services
  • Medical contraindications for immunization

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (phone-based screening and baseline assessment)

Intervention

Duration - 6 weeks

Participants in the intervention group receive a booklet designed to support preventive care decision-making and six telephone-based patient activation sessions over six weeks to promote vaccination uptake and self-management skills.

6 telephone sessions, each around 20 minutes

Control

Duration - 6 weeks

Participants in the control group receive a pamphlet about recommended vaccinations and six control telephone care visits over six weeks focusing on general health advice.

6 telephone visits, each around 5 to 10 minutes

Follow-up Assessments

Duration - 4 months

Participants complete follow-up assessments within 1 month and again at 4 months after the intervention to measure vaccination uptake and changes in health behaviors and attitudes.

2 follow-up assessments (within 1 month and at 4 months post-intervention)

Trial Site Locations

Total: 1 location

1

School of Public Health, The University of Hong Kong

Hong Kong, China, Hong Kong, HKG

Actively Recruiting

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Research Team

Q

Qiuyan Liao

Y

Yuyi Chen

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

The current and potential health benefits of the National Health Service Health Check cardiovascular disease prevention programme in England: A microsimulation study.

Oliver T Mytton, Christopher Jackson, Arno Steinacher...

https://pubmed.ncbi.nlm.nih.gov/29509767

Effectiveness and safety of dual influenza and pneumococcal vaccination versus separate administration or no vaccination in older adults: a meta-analysis.

Mingjuan Yin, Lingfeng Huang, Yan Zhang...

https://pubmed.ncbi.nlm.nih.gov/29961353

Barriers to preventive care utilization among Hong Kong community-dwelling older people and their views on using financial incentives to improve preventive care utilization.

Qiuyan Liao, Wingyan Lau, Sarah McGhee...

https://pubmed.ncbi.nlm.nih.gov/33949749