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Female Genital Schistosomiasis in Tanzania (ShWAB)

Primary Purpose

Schistosomiasis Mansoni

Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
self-collected and operator-collected swab followed by molecular analysis
Sponsored by
IRCCS Sacro Cuore Don Calabria di Negrar
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Schistosomiasis Mansoni focused on measuring Female Genital Schistosomiasis

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Women aged 18-45 years, having had prior sexual activity (to allow speculum-aided gynaecological visit and genital sampling), resident in any of the selected village of Itilima and Maswa districts, irrespective of complaining of urogenital symptoms, not reporting any exclusion criteria, willing to participate to the study as documented by signing the informed consent form. Exclusion Criteria: Menstruation at the time of visit (since this limits visualization of the cervix and correct sampling); no prior sexual activity (since this does not allow the use of a speculum in the visit); known pregnancy; documented treatment for schistosomiasis in the past 6 months; age <18 or >45 years; unwilling to sign the informed consent form.

Sites / Locations

  • IRCCS Sacro Cuore Don Calabria hospital
  • Catholic University of Health and Allied Sciences (CUHAS)

Outcomes

Primary Outcome Measures

Prevalence of Female Genital Schistosomiasis
Prevalence of Female Genital Schistosomiasis among women aged 18-45 years living in selected villages of Itilima and Maswa districts, North-western Tanzania

Secondary Outcome Measures

Acceptability of different sample collection and diagnostic approaches (genital self-sampling, speculum-aided collected genital sampling conducted by female or hypothetically by male healthcare workers)
The participant will be asked some questions about her clinical history and about her experience with self-sampling.
Sensitivity and specificity of self-collected versus healthcare operator speculum-aided collected cervico-vaginal samples for diagnosis of Female Genital Schistosomiasis
Sensitivity of the two genital sampling methods will be calculated using the composite reference constituted by positivity in at least one genital swab, and the performance of the two methods.

Full Information

First Posted
March 3, 2023
Last Updated
March 15, 2023
Sponsor
IRCCS Sacro Cuore Don Calabria di Negrar
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1. Study Identification

Unique Protocol Identification Number
NCT05788003
Brief Title
Female Genital Schistosomiasis in Tanzania
Acronym
ShWAB
Official Title
Female Genital Schistosomiasis in Tanzania: Evaluation of Prevalence and Performance of Schistosoma Haematobium-specific Polymerase Chain Reaction (PCR) on Operator-based and Self-collected Cervical-vaginal Samples Among Women Living in Endemic Areas, North-western Tanzania
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 4, 2022 (Actual)
Primary Completion Date
March 17, 2023 (Anticipated)
Study Completion Date
March 17, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IRCCS Sacro Cuore Don Calabria di Negrar

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A cross-sectional survey will be conducted among 200 volunteering women aged 18- 45 years and having had prior sexual activity living in the target villages of Itilima and Maswa districts, North-western Tanzania. A single midday urine sample and two cervical-vaginal swabs (both self-collected and speculum-aided collected by a female healthcare worker) will be obtained from participating women and processed using urine filtration and polymerase chain reaction (PCR) for cervico-vaginal samples. A pre-tested structure questionnaire will be used to collect sociodemographic, clinical, and sampling acceptability information from participants.
Detailed Description
A cross-sectional survey will be conducted among 200 volunteering women aged 18-45 years and having had prior sexual activity living in the target villages of Itilima and Maswa districts, North-western Tanzania. A single midday urine sample and two cervical-vaginal swabs (both self-collected and speculum-aided collected by a female healthcare worker) will be obtained from participating women and processed using urine filtration and polymerase chain reaction (PCR) for cervico-vaginal samples. A pre-tested structure questionnaire will be used to collect sociodemographic, clinical, and sampling acceptability information from participants. Prevalence of Female Genital Schistosomiasis (FGS) will be estimated based on positivity of at least one genital specimen. Quantitative data will be described using means/medians and standard deviation/interquartile range, as appropriate. Qualitative data will be described as numbers and percentages, and compared using Chi-squared or Fisher Exact test, as appropriate. Sensitivity of the two genital sampling methods will be compared using the composite reference constituted by positivity in at least one genital swab, and the performance of the two methods compared using Cohen's Kappa statistics, Fisher's Exact test and parametric/nonparametric test for comparison of PCR Ct values, as appropriate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schistosomiasis Mansoni
Keywords
Female Genital Schistosomiasis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
206 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Diagnostic Test
Intervention Name(s)
self-collected and operator-collected swab followed by molecular analysis
Intervention Description
A single midday urine sample and two cervical-vaginal swabs (both self-collected and speculum-aided collected by a female healthcare worker) will be obtained from participating women and processed using urine filtration and polymerase chain reaction (PCR) for cervico-vaginal samples.
Primary Outcome Measure Information:
Title
Prevalence of Female Genital Schistosomiasis
Description
Prevalence of Female Genital Schistosomiasis among women aged 18-45 years living in selected villages of Itilima and Maswa districts, North-western Tanzania
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Acceptability of different sample collection and diagnostic approaches (genital self-sampling, speculum-aided collected genital sampling conducted by female or hypothetically by male healthcare workers)
Description
The participant will be asked some questions about her clinical history and about her experience with self-sampling.
Time Frame
6 months
Title
Sensitivity and specificity of self-collected versus healthcare operator speculum-aided collected cervico-vaginal samples for diagnosis of Female Genital Schistosomiasis
Description
Sensitivity of the two genital sampling methods will be calculated using the composite reference constituted by positivity in at least one genital swab, and the performance of the two methods.
Time Frame
6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women aged 18-45 years, having had prior sexual activity (to allow speculum-aided gynaecological visit and genital sampling), resident in any of the selected village of Itilima and Maswa districts, irrespective of complaining of urogenital symptoms, not reporting any exclusion criteria, willing to participate to the study as documented by signing the informed consent form. Exclusion Criteria: Menstruation at the time of visit (since this limits visualization of the cervix and correct sampling); no prior sexual activity (since this does not allow the use of a speculum in the visit); known pregnancy; documented treatment for schistosomiasis in the past 6 months; age <18 or >45 years; unwilling to sign the informed consent form.
Facility Information:
Facility Name
IRCCS Sacro Cuore Don Calabria hospital
City
Negrar
State/Province
Verona
ZIP/Postal Code
37024
Country
Italy
Facility Name
Catholic University of Health and Allied Sciences (CUHAS)
City
Mwanza
Country
Tanzania

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Study data will be shared together with the paper describing the study results.

Learn more about this trial

Female Genital Schistosomiasis in Tanzania

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