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Contact Us → Apply Now →

  • Home
  • About
    • Staff
    • Safety
    • FAQs
    • Location
    • Blog
  • Studies
    • Available Studies
    • Ongoing Studies
  • Enroll
    • Application
    • Study Process
    • How to Participate
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About Clinical Research
Study #52223

Clinical Research Study #52223 will be evaluating the safety and effectiveness of a combined RSV and COVID-19 vaccine with an already marketed flu vaccine in elderly adults.

Are You a Good Fit?

Man or Woman

In general good health

65 years and older

Smokers and non-smokers

  • Receive up to $420 for your participation in this study
Elderly Couple Hugging

What are the Time Requirements?

This study will consist of 1-screening/dosing outpatient visit , 1 follow-up visit and 1 telephone contact. Study dates are as follows:
Group 1
Visit Dates
Stay
Thursday, June 1, 2023 - Thursday, June 1, 2023
Return
Friday, June 30, 2023
Follow-up Phone Call
Monday, November 27, 2023

How Much: $420

Group 2
Visit Dates
Stay
Friday, June 2, 2023 - Friday, June 2, 2023
Return
Wednesday, July 5, 2023
Follow-up Phone Call
Thursday, November 30, 2023

How Much: $420

Group 3
Visit Dates
Stay
Monday, June 5, 2023 - Monday, June 5, 2023
Return
Wednesday, July 5, 2023
Follow-up Phone Call
Thursday, November 30, 2023

How Much: $420

Group 4
Visit Dates
Stay
Tuesday, June 6, 2023 - Tuesday, June 6, 2023
Return
Thursday, July 6, 2023
Follow-up Phone Call
Tuesday, November 28, 2023

How Much: $420

Group 5
Visit Dates
Stay
Wednesday, June 7, 2023 - Wednesday, June 7, 2023
Return
Friday, July 7, 2023
Follow-up Phone Call
Wednesday, November 29, 2023

How Much: $420

Group 6
Visit Dates
Stay
Thursday, June 8, 2023 - Thursday, June 8, 2023
Return
Monday, July 10, 2023
Follow-up Phone Call
Thursday, November 30, 2023

How Much: $420

Group 7
Visit Dates
Stay
Friday, June 9, 2023 - Friday, June 9, 2023
Return
Tuesday, July 11, 2023
Follow-up Phone Call
Friday, December 1, 2023

How Much: $420

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Referral Program

Do not forget our REFERRAL PROGRAM. Earn at least $200 for every new participant you refer who completes a study.*

*No referral bonuses are paid out for outpatient vaccine studies.
elderly couple jumping

All study dates are tentative and subject to change.

We will update the clinical research studies list weekly. Be sure to check with us either by calling or going online. Call (417) 831-2048 or visit 417studies.com for more information. You can also visit the Screening and Recruitment Center located at 2025 W. Sunshine Street, L-109. Office hours are Monday through Friday from 8 a.m. to 5 p.m.

• Eligible individuals must willing and able to comply with all scheduled visits, investigational plan, laboratory tests, lifestyle considerations, and other study procedures.

• Healthy participants are determined by medical history, physical examination, and clinical judgment of the investigator to be eligible for the study.

• Eligible individuals must be capable of giving signed informed consent as described in the protocol, which includes compliance with the requirements and restrictions.

• A female participant is eligible to participate if she is not pregnant or breastfeeding and at least 1 of the following conditions applies:
• Postmenopausal females are defined as no menses for 12 months without an alternative medical cause.
• Is not a WOCBP
• Premenopausal female with 1 of the following:
• Documented hysterectomy;
• Documented bilateral salpingectomy;
• Documented bilateral oophorectomy.

For individuals with permanent infertility due to a medical cause other than the above (eg, mullerian agenesis, androgen insensitivity), investigator discretion should be applied to determining study entry.

• Is a woman of Child Bearing Potential
• Highly Effective Methods That Have Low User Dependency:
• Implantable progestogen only hormone contraception associated with inhibition of ovulation.
• Intrauterine device.
• Intrauterine hormone releasing system.
• Bilateral tubal occlusion.
• Vasectomized partner:
• Vasectomized partner is a highly effective contraceptive method provided that the partner is the sole sexual partner of the WOCBP and the absence of sperm has been confirmed. If not, an additional highly effective method of contraception should be used. The spermatogenesis
cycle is approximately 90 days.

• Highly Effective Methods That Are User Dependent:
• Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation:
• Oral;
• Intravaginal;
• Transdermal.
• Progestogen only hormone contraception associated with inhibition of ovulation:
• Oral
• Injectable
• Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study intervention. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the
study and the preferred and usual lifestyle of the participant.

• Other Effective Methods
• Progestogen only oral hormonal contraception where inhibition of ovulation is not the primary mode of action.
• Male or female condom, with or without spermicide.
• Cervical cap, diaphragm, or sponge with spermicide.
• A combination of male condom with either cervical cap, diaphragm, or sponge with spermicide (double barrier methods

If you have previously submitted an application, call 417-831-2048 to enroll. Or click on the button below to submit your application now.

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QPS Missouri

QPS Study Campus
1820 W. Mount Vernon Street
Springfield, MO 65802

QPS Screening and Recruitment Center
2025 W. Sunshine Street, L-109
Springfield, MO 65807

Hours of Operation:
Monday – Friday
8 a.m. – 5 p.m.

Call us at 417.831.2048

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