Family Physician Nudges for Influenza Vaccination Among Older Adults

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55+
SponsorFudan University

About this trial

The goal of this clinical trial is to learn if a family-physician nudge intervention works to improve influenza vaccination among adults aged 55 years and older in China. Three independent, parallel cluster randomized controlled trials will be conducted under three distinct vaccine payment policies, i.e. free vaccination for those older than 65 years and self-paid vaccination for those \<65 years in rural areas, and partially insurance-covered vaccination in urban areas.

The main questions it aims to answer are:

1. Does the family-physician nudge intervention increase influenza vaccination uptake among older adults? How does the effectiveness of the nudge intervention vary under different payment policies? 2. Is the family-physician nudge intervention cost-effective, acceptable, feasible, and potentially sustainable in primary care settings? Researchers will compare an intervention group receiving a family-physician nudge with a control group receiving routine care to see if the nudge is effective at increasing influenza vaccination among older adults.

Participants will:

1. Be recruited at community health service centers and cluster-randomized by their family physicians into one of two groups. 2. Receive either a physician nudge (provider recommendation by an endowment-framing educational pamphlet + default appointment + a follow-up reminder) or routine health education. 3. Have their influenza vaccination status verified through the immunization information system at the end of the trial.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age ≥ 55 years.

Not vaccinated against influenza in the current flu season.

No contraindications to influenza vaccination.

Willing and able to provide informed consent and participate in the study.

Disqualifiers

Age under 55 years.

Has already received influenza vaccination in the current flu season.

Has a known contraindication to influenza vaccination.

Unable to comply with study procedures.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Family Physician Influenza Vaccination Nudge

    Behavioral

    A family-physician-delivered behavioral nudge combines provider recommendation by an endowment-framing educational pamphlet, default appointment scheduling, and a follow-up reminder, which is designed to increase influenza vaccination uptake among older adults. Grounded in behavioral science theories of vaccination decision-making and nudging, the intervention leverages the high credibility of primary-care family physicians among older adults and reduces the behavioral frictions associated with seeking vaccination.

Treatment groups

5,250 Participants
are divided into 2 treatment groups
Group A: Family Physician Nudge GroupExperimental treatment 1 intervention
Group B: Routine Care GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Influenza Vaccination Uptake

Whether participants get vaccinated against influenza, measured by official vaccination records.

Time frame
1 month and 3 months after the intervention

Secondary outcomes

1

Timing of Influenza Vaccination

Number of days from the intervention date to receipt of influenza vaccination, measured by official vaccination records.

Time frame
Within 3 months after the intervention

Other outcomes

1

Spouse Influenza Vaccination Uptake

Whether the participant's spouse gets vaccinated against influenza, measured by official vaccination records.

Time frame
1 month and 3 months after the intervention
2

Timing of Spouse Influenza Vaccination

Number of days from the participant's intervention date to spouse's influenza vaccination, measured by official vaccination records.

Time frame
Within 3 months after the intervention
3

Incremental Cost-Effectiveness Ratio (ICER)

Cost per additional vaccinated person and cost per additional quality-adjusted life year (QALY) gained, calculated from both health-system and societal perspectives using micro-costing data. QALYs projected over annual horizon.

Time frame
Within 3 months after the intervention

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: