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Uterine Cervical CancerNCT01299714

Community Awareness, Resources and Education (CARE II): Project 3

An observational study of Uterine Cervical Cancer, run by Ohio State University Comprehensive Cancer Center at 4 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Researchers at The Ohio State University and the University of Michigan are working together to understand cancer of the cervix. One of the areas they are studying is how stress you may experience in your life effects the way you respond to GARDASIL®. Read more about this study

Who is it for?
Ages 18 to 26 years, women onlyHealthy volunteers can take part
Conditions the study is for
Uterine Cervical Cancer
How many people
191 participants
Where
4 sitesUnited States
Study dates
Feb 2011to Apr 2015
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 26 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Study population: Participants will be female, aged 18 - 26 years, residing in an Appalachian region, with no history of HPV vaccination.

Who may be able to join

  • Female
  • 18-26 years of age
  • Resident of an Appalachian county
  • Intact cervix
  • Able to read and understand English
  • Cognitively able to provide informed consent
  • Willing to come for four clinic visits

Who cannot join

  • Prior history of cervical cancer
  • Prior history of a cervical lesion treated with cryotherapy or any form of surgical removal of a portion of the cervix to treat CIN
  • No cervix
  • Pregnant or planning to become pregnant in the next year
  • History of immune disorder: auto-immune, primary immune or acquired
  • Any contra-indications for the GARDASIL® vaccine series
Show all 9Show fewer
  • Taking immune suppressive medications
  • Any prior exposure to an HPV vaccine of any type
  • Planning to move out of the immediate area in the next year

Trial locations and contacts

4 sites in 1 country.

United States4 sites
  • Study site

    Athens, Ohio, 45701

  • Study site

    Gallipolis, Ohio, 45631

  • Study site

    Logan, Ohio, 43138

  • Study site

    Pomeroy, Ohio, 45769

Other trials in United States

About this study

Researchers at The Ohio State University and the University of Michigan are working together to understand cancer of the cervix. One of the areas they are studying is how stress you may experience in your life effects the way you respond to GARDASIL®. GARDASIL® is a vaccine approved by the Food and Drug Administration (FDA) to prevent some types of Human Papillomavirus (HPV) infection which can cause cancer of the cervix. Participants are being recruited from the Appalachian region of Ohio.

Read the detailed description

A quadrivalent HPV 6, 11, 16, 18 vaccine (GARDASIL®) has been approved for use among women age 9-26 years to prevent cervical/vaginal/vulvar cancer and genital warts. The efficacy of the vaccine has been demonstrated in clinical trial settings, but the effectiveness of this vaccine has not been tested in clinical practice settings. Patients experiencing greater stress have a reduced capacity to mount an immune response to other types of vaccine. The same phenomenon is likely to exist for Gardasil, but there are no data. The impact of psychological stress on the immune response to a vaccine is proposed to act via health behaviors (multiple lifetime sexual partners, never using condoms, prior abnormal Pap smear, smoking, and HPV infection) or by direct dysregulation of the immune system. We have found higher rates of cervical HPV in Appalachian Ohio women, higher rates of abnormal cervical cytology, and very high rates of psychological stress compared to urban and suburban women. The goal of this study is to determine if, in women age 18-26 years given GARDASIL® vaccine, serum HPV 6/11/16/18 antibody response is altered by stress. This will be accomplished by a study of 432 women age 18-26 years who report full range of life stressors recruited from Appalachian Ohio. All participants will receive the GARDASIL® vaccine at baseline, two months, and six months. Prior to vaccination questionnaire data related to HPV exposure risk behaviors and psychological stressors will be collected. Cervical samples will be collected for cytology and HPV testing. Serum samples will be collected for HPV 6, 11, 16 and 18 antibody assays at baseline and month 12. The questionnaire data and serum samples will be repeated at 12 months. The primary outcome measure is the difference in serum antibodies to HPV 6, 11, 16 and 18 at baseline and month 12. The variables of interest are perceived stress, sexual behaviors, socioeconomic status, access to health care (health insurance yes/no), smoking, Appalachian self-identity, HPV cervical status at baseline, and past history abnormal cervical cytology, as proposed in a psychoneuroimmunology model. In this model, Appalachian Self-Identity, socioeconomic status, loneliness, health care access, and coping are proposed to contribute to a woman's perceived stress. The impact of perceived stress on immune response to Gardasil vaccination can be by health behaviors such as multiple lifetime sexual partners (>4), never using condoms, prior abnormal Pap smear, smoking, and HPV status at the time of vaccination. Perceived stress can have a direct physiologic impact on the immune response by creating immune dysregulation as measured by increased EBV VCA-IgG titers. Depressive symptoms can mediate the impact of perceived stress on immune function. If psychological stress is found to modulate the immune response to GARDASIL®, then we can determine if the modulation reduces the clinical effectiveness of the vaccine and examine methods to limit the impact of stress.

Keywords
Human Papilloma Virus, vaccine, stress, cervical cancer, GARDASIL
Medical subject headings
Uterine Cervical Neoplasms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. serum antibody levels for HPV 6,11,16 and 18

    Measured: 12 months

Secondary outcomes (3)
  1. serum antibody levels for Epstein-Barr Virus (EBV)

    Measured: baseline

  2. Center for Epidemiological Studies - Depression (CES-D) Scale Score

    Measured: 12 months

  3. perceived stress

    Measured: 12-months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Feb 2011 (estimated)
  2. Study startFeb 2011
  3. Primary completionNov 2014
  4. Study completionApr 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
191 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01299714
Sponsor's protocol ID
OSU-10096
Other IDs
P50CA105632, OSU-10096
Status last verified
Apr 2018
First submitted
15 Feb 2011
Last updated
25 Apr 2018
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Uterine Cervical Cancer, run by Ohio State University Comprehensive Cancer Center at 4 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Apr 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

serum antibody levels for HPV 6,11,16 and 18 (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Apr 2018; AzTrials last refreshed its copy on 6 Nov 2026.

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