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Not yet recruitingNCT07871448Updated Oct 13, 2026

Flu COVID Vaccine Views

An observational study in Influenza, COVID-19 and Vaccination Willingness, sponsored by George Washington University. Not yet recruiting at 2 sites in United States. Open to participants aged 18 Years to 89 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by George Washington University · Observational

Updated Oct 13, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
550
Ages
18 Years to 89 Years
Sex
All
01

Study summary

This study addresses a critical evidence gap relevant to implementation strategies for combination vaccines in health care settings. This study will specifically investigate healthcare worker (HCWs) attitudes around and willingness to receive combination influenza/COVID-19 vaccines. Findings will identify determinants of hesitancy and acceptance among HCWs and support effective rollout strategies and communication approaches. Cross-sectional surveys and qualitative interviews will be conducted with healthcare workers to characterize HCW willingness to be vaccinated and to identify demographic, attitudinal, and structural predictors of vaccination.

Read the detailed description

This study uses a sequential explanatory mixed-methods design. The first phase utilizes a cross-sectional, multi-site electronic survey. The quantitative survey will characterize willingness of approximately 550 HCWs to receive a combination influenza/COVID-19 vaccine and to identify demographic, attitudinal, and structural predictors of vaccination. Participants will complete a one-time REDCap survey (approximately 20-30 minutes).

In the second phase, a subset of 10-20 HCWs will be invited to participate in qualitative interviews that will be used to interpret and elaborate on quantitative findings. Specifically, the qualitative analysis allows for exploration of the nuanced rationale behind reported willingness to vaccinate, gives additional context to latent constructs identified in factor analysis, and identifies communication preferences that are not adequately captured by closed-ended questions. Integration will occur at the interpretation stage: quantitative results will inform purposive sampling for the qualitative phase, and qualitative themes will be used to contextualize and explain patterns observed in the quantitative analysis. A joint display table will be used in reporting to show how qualitative findings confirm, extend, or challenge quantitative results.

02

Conditions studied

  • Influenza
  • COVID-19
  • Vaccination Willingness
03

In context

Influenza, Human

2,264 studies on the registry are indexed under Influenza, Human; 173 are open to participants now.

This study's planned enrollment of 550 is above the median of 300 across 313 observational studies indexed under Influenza, Human.

Browse Influenza, Human studies →

Lead sponsor

George Washington University is the lead sponsor of 191 studies on the registry; 34 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 11 (85%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 89 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Healthcare workers who are eligible for seasonal influenza vaccination, encompassing both clinical and non-clinical positions (physicians, advanced practice providers, nurses, allied health professionals, administrative and support staff, trainees, and students). We are targeting enrollment of 275 participants per site (George Washington University and Children's National Hospital), for a study-wide total of 550.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18-89 years old
  • Currently employed or enrolled as a student at GWU, GW MFA or CNH
  • Eligible for institutional influenza vaccination
  • Able to complete the survey in English

Exclusion criteria

Exclusion Criteria:

  • On long-term leave at the time of survey launch
  • Contractors without institutional email access
  • Contraindication to receiving influenza vaccination
  • Contraindication to receiving COVID-19 vaccination
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
550 participants (estimated)
Patient registry
No

Interventions

  • OtherSurvey

    One-time RedCAP electronic survey on the willingness of healthcare workers to receive a combination influenza/COVID-19 vaccine and factors that might influence this decision.

06

What researchers measure

Primary outcomes

  1. Proportion of health care workers (HCWs) who indicate that they would "definitely" or "probably" receive a combination influenza and COVID-19 vaccine.

    Time frame: Day 1

Secondary outcomes

  1. Proportion of HCWs willing to receive standalone seasonal influenza vaccines.

    Time frame: Day 1

  2. Proportion of HCWs willing to receive standalone COVID-19 vaccines, also stratified by COVID-19 vaccine platform (mRNA vs. protein-based).

    Time frame: Day 1

  3. Determinants of willingness to receive combination influenza and COVID-19 vaccines as assessed by multivariable logistic regression.

    Adjusted odds ratios (aOR) for demographic, occupational, behavioral, attitudinal, and emotional predictors associated with vaccination willingness, measured using responses from the REDCap electronic survey.

    Time frame: Day 1

  4. Categorization of attitudes toward co-administration compared with true combination vaccine formulations as assessed by semi-structured qualitative interviews.

    Qualitative thematic analysis of healthcare worker attitudes and preferences recorded using a semi-structured qualitative interview guide.

    Time frame: Day 1 through completion of the qualitative surveys, an average of 1 month.

  5. Participant ranking of messaging options associated with willingness to receive combination vaccines as assessed by REDCap survey.

    Mean ranking scores of communication messaging options measured via ordinal ranking items in the REDCap electronic survey.

    Time frame: Day 1 through completion of the qualitative surveys, an average of 1 month.

  6. Proportion of participants in different thematic categories regarding concerns, motivations, and preferred communication strategies as assessed by qualitative thematic analysis.

    Identified qualitative themes and sub-themes synthesized using qualitative thematic analysis from REDCap survey free-text fields and semi-structured interview transcripts.

    Time frame: Day 1 through completion of the qualitative surveys, an average of 1 month.

  7. Proportion of participants in different thematic categories associated with willingness to receive combination vaccines as assessed by semi-structured qualitative interviews.

    Qualitative themes identified through inductive thematic analysis of semi-structured interview transcripts.

    Time frame: Day 1 through completion of the qualitative surveys, an average of 1 month.

07

Study locations

2 sites
  • Children's National Hospital
    Washington D.C., District of Columbia 20020, United States
  • George Washington University
    Washington D.C., District of Columbia 20037, United States
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07871448
Responsible party
Daniel Park (Senior Research Scientist, George Washington University) — Principal investigator
First posted
Oct 13, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Sep 30, 2027 (estimated)
Completion
Apr 1, 2028 (estimated)
Last update
Oct 13, 2026

Study contacts

Daniel Park, PhD
Contact
danpark@email.gwu.edu
202-994-0218
Annie Roberts
Contact
610-283-4402
Daniel Park, PhD
principal investigator · George Washington University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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