- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06818123
Exploring the Effectiveness of Interventions on Menstrual Hygiene Awareness in Slum Communities of Karachi, A Quasi- Experimental Analysis
February 5, 2025 updated by: SINA Health Education and Welfare Trust
Exploring the Effectiveness of Interventions on Menstrual Hygiene Awareness in Slum Communities of Karachi, A Quasi- Experimental Analysis.
Proper menstrual hygiene knowledge and practices are crucial among women.
People of urban slum's areas have no or less knowledge and practices of Menstruation hygiene due to low socio-economic status.
This study helps in Improving menstrual hygiene knowledge and practices and can empower individuals to manage their periods with dignity and comfort.
This study also contributes in creating a more open and supportive environment for menstruation by addressing stigma and misconception.
The study also helps in reducing the risk of reproductive tract infections.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Interventional
Enrollment (Estimated)
400
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hina Sharif, Pharm-D, MBA, MSPH
- Phone Number: +922136943376
- Email: hina.sharif@sina.pk
Study Contact Backup
- Name: Sana S Sheikh, MSc. MPH
Study Locations
-
-
Sindh
-
Karachi, Sindh, Pakistan, 74800
- SINA Health Education and Welfare Trust
-
Contact:
- Sana S Sheikh, Msc.,MPH
- Email: sanshf4@gmail.com
-
Contact:
- Hina Sharif, Pharm-D,MBA,MSPH
- Phone Number: 03332109679
- Email: hina.sharif@sina.pk
-
Principal Investigator:
- Hina Sharif, Pharm-D,MBA,MSPH
-
Sub-Investigator:
- Tooba Seemi, MSc.
-
Sub-Investigator:
- Sana S Sheikh, MSc. MPH
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Woman age in between 15-45years of age
- Those who used reusable items for menstruations
- Those who are willing to participate voluntarily will be included in the study
Exclusion Criteria:
- Participants who are suffering from any serious medical condition.
- live in other than slums area of Karachi will be excluded from the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Control Arm
Education Intervention along with the doctor's consultation
|
Baseline Knowledge will be assessed in this arm about the menstruations hygiene and practices.
|
|
Experimental: Intervention
Those who will be under the baseline screening in term of knowledge, will then treated as interventional arm and interventional will be given to them.
|
This educational intervention will assess the improvement menstrual hygiene knowledge and practices among women at slums who are illiterate and can empower individuals to manage their periods with dignity and comfort.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improved Menstruations Hygiene knowledge
Time Frame: one month
|
Effectiveness of educational intervention of menstruation hygiene among participants
|
one month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reduction in vaginal infection
Time Frame: one month
|
Recurrent Infection such as yeast infection, discomfort, itching, other related infection.
|
one month
|
|
promoting better self-esteem and confidence
Time Frame: one month
|
Participants who is taking the education session and counselling, adapt the good women hygiene
|
one month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 28, 2025
Primary Completion (Estimated)
March 31, 2025
Study Completion (Estimated)
April 15, 2025
Study Registration Dates
First Submitted
September 28, 2024
First Submitted That Met QC Criteria
February 5, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 5, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 0006
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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