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Trial record 40 of 12451 for:    cervical

The Kilimanjaro Cervical Screening Project (KCCP)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01968837
Recruitment Status : Completed
First Posted : October 24, 2013
Last Update Posted : April 13, 2016
Sponsor:
Collaborators:
Grand Challenges Canada
Kilimanjaro Christian Medical Centre, Tanzania
Information provided by (Responsible Party):
Dr. Karen Yeates, Queen's University

Brief Summary:
Although highly curable, cervical cancer kills thousands of women in developing countries annually. The investigators will pilot a project to improve detection of cervical cancer in Kilimanjaro, Tanzania through a program that combines access to cervical screening expertise available in a large medical centre and remote use of a mobile phone camera application.

Condition or disease Intervention/treatment Phase
Uterine Cervical Neoplasms Cervical Cancer Other: Cervical cancer screening Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 1072 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Screening
Official Title: The Kilimanjaro Cervical Screening Project
Study Start Date : May 2014
Actual Primary Completion Date : September 2015
Actual Study Completion Date : September 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cervical Cancer

Arm Intervention/treatment
No Intervention: Cervical cancer screening Other: Cervical cancer screening



Primary Outcome Measures :
  1. Test accuracy of using digital smart phone cervicograms in place of traditional cervicography images produced through traditional SLR cameras [ Time Frame: 3 months ]

Secondary Outcome Measures :
  1. Measure accuracy and feasibility of non-physician healthcare workers ability to obtain adequate cervical images via smart phone camera photographs. [ Time Frame: 3 months ]

Other Outcome Measures:
  1. Measure accuracy, quality, and feasibility of SMS text messaging of cervical images obtained by smart phone in place of traditional transfer methods for digital cervical images. [ Time Frame: 3 months ]


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Ages Eligible for Study:   25 Years to 49 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Female
  • Over 18 years of age

Exclusion Criteria:

  • Previous removal of uterus

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01968837


Locations
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Tanzania
Reproductive Health Centre, KCMC
Moshi, Tanzania
Sponsors and Collaborators
Queen's University
Grand Challenges Canada
Kilimanjaro Christian Medical Centre, Tanzania
Investigators
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Principal Investigator: Karen Yeates, MD Queen's University

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Responsible Party: Dr. Karen Yeates, Associate Professor, Department of Medicine, Queen's University
ClinicalTrials.gov Identifier: NCT01968837     History of Changes
Other Study ID Numbers: DMED-1545-12
First Posted: October 24, 2013    Key Record Dates
Last Update Posted: April 13, 2016
Last Verified: April 2016

Additional relevant MeSH terms:
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Uterine Cervical Neoplasms
Uterine Neoplasms
Genital Neoplasms, Female
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Uterine Cervical Diseases
Uterine Diseases
Genital Diseases, Female