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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05709951
Other study ID # RiphahIU fatimatariq1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2022
Est. completion date February 2023

Study information

Verified date January 2023
Source Riphah International University
Contact Fatima Tariq, Phd
Phone 03344255033
Email fatima.tariq@riphah.edu.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the effects of Functional and Core stability exercises on pain and sleep quality in Patients with Primary Dysmenorrhea and to check the results of exercises may be effective in pain during Menstrual and before cramping in menses.


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date February 2023
Est. primary completion date February 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 30 Years
Eligibility Inclusion Criteria: - Having used medication for menstrual pain and not having used oral contraceptives during the three months prior to admission to the study. - Pain must be periodic (at least following 3 menstrual cycles). - Lower abdominal cramps pain ends after periods and gradually diminish over 12 to 72 hrs. - No history of blood disorders including thalassemia and folate or iron-deficiency anemia Exclusion Criteria: - Pelvic inflammatory disease - Ovarian cysts - Chronic abdominal pain - Fibroids, obstructive endometrial polyps, - Irritable bowel syndrome - Major abdominal or pelvic surgery - Intrauterine devices.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Functional Exercises
The patients were requested to perform these functional exercises for 4 days per week three times for 20 min (8 weeks).
Core Stability Exercises
The patients were requested to perform 4 core strengthening exercises for 4 days per week three times for 20 min (8 weeks)

Locations

Country Name City State
Pakistan Jinnah Hospital Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analogue scale for lower abdominal pain The subjective and verified visual analogue scale is used to quantify both acute and chronic pain (1). On the 10 cm line, scores are recorded by making a mark. Pain intensity is measured along a 10-cm line with 0 denoting "no pain" and 10 denoting "worst pain." 8 week
Primary Menstrual Symptom Questionnaire Menstrual Symptom Questionnaire (MSQ) to assess dysmenorrhea symptoms. The MSQ is a 24 item self-report measure which assesses menstrual pain and symptoms (e.g. 'I have cramps that begin on the first day of my period'; 'I feel depressed for several days before my period'). The score on each item ranges from 1 (never) to 5 (always) with a higher composite score indicating more symptoms. 8 weeks
Primary Pittsburgh Sleep Quality Index Pittsburgh Sleep Quality Index (PSQI) evaluates sleep disruptions and quality over a 1-month period. In scoring the PSQI, seven component scores are derived, each scored 0 (no difficulty) to 3 (severe difficulty). 8 week
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