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The Development of a "Mother/Child, Screen, Treat and Vaccinate Program" in Manchay and Iquitos, Peru (PERCAPS)

Primary Purpose

Cervical Intraepithelial Neoplasia, Cervical Cancer, Cervical Neoplasm

Status
Completed
Phase
Phase 1
Locations
Peru
Study Type
Interventional
Intervention
Gardasil
Sponsored by
Preventive Oncology International, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cervical Intraepithelial Neoplasia focused on measuring Community based participatory research

Eligibility Criteria

30 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

Inclusion criteria (adult)

  1. Non pregnant women 30-45 years of age in Manchay, and in Iquitos, with female children or grandchildren ages 10-13 who they are willing to enroll in the study to receive Gardasil vaccination.
  2. No screening or knowledge of the results of a Pap Test in the last 5 years
  3. No hysterectomy
  4. No prior pelvic radiation.
  5. Willing to sign consent form

Inclusion criteria (children)

  1. Female children and grandchildren of a participating women ages 10-13 years
  2. No acute illnesses (clinically evident according to vaccinating staff) - such as fever, nausea, vomiting, diarrhea
  3. No previous vaccination with Gardasil
  4. No reactions to previous dose in their vaccination series
  5. No known yeast allergy
  6. Willing to participate

Exclusion Criteria:

Exclusion criteria (adults)

Patients will be excluded in the study based on the following criteria:

  1. Males
  2. Women younger than 30 years old and older than 45 years old.
  3. Women without female children or grandchildren age 10-13 or who are unwilling to enroll their 10-13 year old female children or grandchildren to receive Gardasil.
  4. Pregnant women.
  5. Patients with known history of hysterectomy or radiation for a pelvic cancer.
  6. Refusal to participate

Exclusion criteria (Children)

  1. Males
  2. Girls younger than 10 years old, and older than 13 years.
  3. acute illnesses (clinically evident according to vaccinating staff) - such as fever, nausea, vomiting, diarrhea
  4. previous vaccination with Gardasil
  5. reactions to a previous dose in their vaccination series
  6. known yeast allergy
  7. Refusal to participate

Sites / Locations

  • Centro de Salud Portada de Manchay
  • Centro de Salud Bellavista Nanay

Outcomes

Primary Outcome Measures

Evaluation of key study processes used in the process of implementing a mother/child screen, treat and vaccinate program in Iquitos, Peru.
The investigators will evaluate community participation, lost to follow up and potential sustainability. One on one interviews with participants will be conducted by trained medical staff. Additional measures to success will be gathered from interviews with promotoras, participating health services staff and recoeded observation. These analyses are descriptive in nature.

Secondary Outcome Measures

Full Information

First Posted
April 16, 2011
Last Updated
April 16, 2014
Sponsor
Preventive Oncology International, Inc.
Collaborators
Peru Instituto Nacional de Enfermadades Neoplasticas (INEN), Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT01338051
Brief Title
The Development of a "Mother/Child, Screen, Treat and Vaccinate Program" in Manchay and Iquitos, Peru
Acronym
PERCAPS
Official Title
The Development of a "Mother/Child, Screen, Treat and Vaccinate Program" in Manchay and Iquitos, Peru (PERCAPS)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Preventive Oncology International, Inc.
Collaborators
Peru Instituto Nacional de Enfermadades Neoplasticas (INEN), Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This project will use a community based participatory research orientation to develop a model for large scale "campaign" preventive healthcare interventions. The investigators have considerable expertise with cervical cancer screening and HPV vaccination. The investigators also have well tested methodologies for cervical cancer screening that are highly effective, including self-sampling for HPV and improved specimen transport systems. Therefore, the investigators will use these medical interventions as the model preventive health interventions for this project.
Detailed Description
Our research group has recently demonstrated that a self-collected cervico-vaginal sample tested with a very high throughput HR-HPV assay is as sensitive has a direct endocervical physician collected sample. Teamed with a non-liquid transport media the investigators believe the technology is solved to reach large populations in a short period of time. With the majority of the world's medically underserved now living in middle income countries it is not necessary to think simple and small to reach the Earth's needy. The investigators can think high tech and high throughput. The massive volumes possible, with proper organization, will control the per/patient cost. The investigators will think "events", not continuous care. Clearly continuous care is the only way to adequately provide the needed care for many problems. However, many interventions can be confined to events which organize large screening or vaccination days and only when positives are identified from the detection algorithm does the healthcare staff become involved for management. The investigators spend an enormous amount of resources identifying the majority of people who will ultimately test negative. The more local the paradigms and the more involved the community in designing the program, the greater will be the participation and the lost to follow-up segment will shrink. This mother, child, screen, treat and vaccinate program will use cervical cancer prevention as the target preventive healthcare intervention. Using community based research orientation the project will begin with a 3 day education program and collaborative meeting with the women leaders of the communities (promotoras). Collectively the investigators will develop the model for the community to advertise, educate, recruit, register, self-collect the specimens, deliver the samples, and report the results. In addition the logistics of the 3 vaccination schedule for the female children will be organized. The medical staff will be involved only with the management of the positives and the vaccine administration. The observational measures will focus on assessing how effectively each of the steps was accomplished.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Intraepithelial Neoplasia, Cervical Cancer, Cervical Neoplasm, Cervical Dysplasia, Human Papillomavirus
Keywords
Community based participatory research

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
642 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Gardasil
Intervention Description
Gardasil will be administered to 10-13 year old daughters and granddaughters of study participants according to manufacturers recommended schedule of administration. Gardasil is supplied as 0.5-mL suspension for intramuscular injection at the following schedule: 0, 2 months, 6 months. DOSAGE FORMS AND STRENGTHS • 0.5-mL suspension for injection as a single-dose vial and prefilled syringe.
Primary Outcome Measure Information:
Title
Evaluation of key study processes used in the process of implementing a mother/child screen, treat and vaccinate program in Iquitos, Peru.
Description
The investigators will evaluate community participation, lost to follow up and potential sustainability. One on one interviews with participants will be conducted by trained medical staff. Additional measures to success will be gathered from interviews with promotoras, participating health services staff and recoeded observation. These analyses are descriptive in nature.
Time Frame
Interview with participants will occur at approximately one month after 2nd vaccination

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Inclusion criteria (adult) Non pregnant women 30-45 years of age in Manchay, and in Iquitos, with female children or grandchildren ages 10-13 who they are willing to enroll in the study to receive Gardasil vaccination. No screening or knowledge of the results of a Pap Test in the last 5 years No hysterectomy No prior pelvic radiation. Willing to sign consent form Inclusion criteria (children) Female children and grandchildren of a participating women ages 10-13 years No acute illnesses (clinically evident according to vaccinating staff) - such as fever, nausea, vomiting, diarrhea No previous vaccination with Gardasil No reactions to previous dose in their vaccination series No known yeast allergy Willing to participate Exclusion Criteria: Exclusion criteria (adults) Patients will be excluded in the study based on the following criteria: Males Women younger than 30 years old and older than 45 years old. Women without female children or grandchildren age 10-13 or who are unwilling to enroll their 10-13 year old female children or grandchildren to receive Gardasil. Pregnant women. Patients with known history of hysterectomy or radiation for a pelvic cancer. Refusal to participate Exclusion criteria (Children) Males Girls younger than 10 years old, and older than 13 years. acute illnesses (clinically evident according to vaccinating staff) - such as fever, nausea, vomiting, diarrhea previous vaccination with Gardasil reactions to a previous dose in their vaccination series known yeast allergy Refusal to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jerome L Belinson, MD
Organizational Affiliation
Preventive Oncology International
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Carlos Vallejos Sologuren, MD
Organizational Affiliation
Instituto Nacional de Enfermadades Neoplasticas (INEN)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro de Salud Portada de Manchay
City
Manchay
State/Province
Lima
Country
Peru
Facility Name
Centro de Salud Bellavista Nanay
City
Iquitos
State/Province
Loreto
ZIP/Postal Code
065
Country
Peru

12. IPD Sharing Statement

Citations:
PubMed Identifier
23385153
Citation
Levinson KL, Abuelo C, Salmeron J, Chyung E, Zou J, Belinson SE, Wang G, Ortiz CS, Vallejos CS, Belinson JL. The Peru Cervical Cancer Prevention Study (PERCAPS): the technology to make screening accessible. Gynecol Oncol. 2013 May;129(2):318-23. doi: 10.1016/j.ygyno.2013.01.026. Epub 2013 Feb 4.
Results Reference
derived
Links:
URL
http://www.poiinc.org
Description
Preventive Oncology International

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The Development of a "Mother/Child, Screen, Treat and Vaccinate Program" in Manchay and Iquitos, Peru

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