- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04852627
Effect of Brisk Walking on Primary Dysmenorrhea
September 4, 2022 updated by: Ain Shams University
Effect of Brisk Walking on Primary Dysmenorrhea Among Medical Students
Dysmenorrhea is a common problem in women.
Exercise is commonly cited as a possible remedy.
We will measure the effect of brisk walking on primary dysmenorrhea among medical students.
Study Overview
Study Type
Interventional
Enrollment (Actual)
170
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 Locations
-
-
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Cairo, Egypt, 002
- AinShams Maternity Hospital
-
-
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
17 years to 25 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- BMI: 18-25
- regular menstrual cycles
Exclusion Criteria:
- Marriage or previous sexual activity
- medical disorders
- previous abdominal or pelvic surgery
- skeletal disorders
- hormonal or psychiatric treatment
- atheletes
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control group
No intervention
|
|
Active Comparator: Exercise group
Will brisk walk 30 minutes 3 times weekly
|
Walking
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dysmenorrhea score
Time Frame: 3 months
|
WaLIDD (working ability, location, intensity, days of pin, dysmenorrhea)score for dysmenorrhea.
Least is 0, highest is 12.
The higher the score, the worse dysmenorrhea
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maii Nawara, MD, Ain Shams University
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 (Actual)
April 24, 2021
Primary Completion (Actual)
February 12, 2022
Study Completion (Actual)
May 20, 2022
Study Registration Dates
First Submitted
April 17, 2021
First Submitted That Met QC Criteria
April 17, 2021
First Posted (Actual)
April 21, 2021
Study Record Updates
Last Update Posted (Actual)
September 7, 2022
Last Update Submitted That Met QC Criteria
September 4, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- M D 59/2021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
IPD will be available with the principal investigator and will be shared if requested
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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