- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05258253
Effects of HIA and PCE in Primary Dysmenorrhea
February 25, 2022 updated by: Riphah International University
Effects of High Intensity Aerobics and Pelvic Clock Exercises in Primary Dysmenorrhea
The main purpose of study is to manage the unpleasant pain suffered by females during Mensturation.
The aim of this study is to guide physiotherapist that how to apply these exercises to manage dysmenorrhea.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
There are less research on effectiveness of pelvic clock exercises in dysmenorrhea they are very less evidence and less documented in literature..
Although there are many researches on high intensity aerobics.Previous researches only have lierature about aerobics.So to address this literature gap, conduct a prospective randomized controlled trial to investigate the effects of high intensity aerobics and pelvic clock exercises in primary dysmenorrhea.
Study Type
Interventional
Enrollment (Actual)
28
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
-
-
Punjab
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Hafizabad, Punjab, Pakistan, 140111
- Rasheeda gynae 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 24 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Girls aged 17-23 years with regular menstrual cycle
- Unmarried girls
Exclusion Criteria:
- Athletes, Married women,
- Girls who were regularly exercising
- Having any pelvic pathology, abnormal menstrual cycle.
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: high intensity aerobics
"London bridges (8mins)","Jumping lunges(8mins)","Mountain climbers(8mins)","Quadruped bent knee hip extension (8mins)"
|
"London bridges (8mins)" "Jumping lunges(8mins)" "Mountain climbers(8mins)" "Quadruped bent knee hip extension (8mins)"
|
Active Comparator: pelvic clock exercises
Lie with your back on the floor in a neutral position with your legs bent and toes facing forward.
Subject begin with gentle movements from 12 to 6 o'clock, as instructed to move from 3 o'clock to 9 o'clock.
Then move in a clockwise manner from 12 to 3 to 6 to 9 and then back to 12 o' clock.
|
Lie with your back on the floor in a neutral position with your legs bent and toes facing forward.
Subject begin with gentle movements from 12 to 6 o'clock, as instructed to move from 3 o'clock to 9 o'clock.
Then move in a clockwise manner from 12 to 3 to 6 to 9 and then back to 12 o' clock.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual analogue scale
Time Frame: last 1 day
|
Scores are recorded by making a mark on a 10-cm line that represents a continuum between "no pain" and "worst pain."
|
last 1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
DASS 21
Time Frame: last 1 day
|
DASS-21 scale contains 7 items, divided into subscales with similar content.
|
last 1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sara Aabroo, PPDPT, Riphah International 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)
February 8, 2021
Primary Completion (Actual)
July 13, 2021
Study Completion (Actual)
November 13, 2021
Study Registration Dates
First Submitted
February 20, 2022
First Submitted That Met QC Criteria
February 25, 2022
First Posted (Actual)
February 28, 2022
Study Record Updates
Last Update Posted (Actual)
February 28, 2022
Last Update Submitted That Met QC Criteria
February 25, 2022
Last Verified
February 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/Lhr/21/0505 Asmaa Qamar
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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