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Combined Effects of Kegel Exercises and 4-7-8 Breathing Technique in Primary Dysmenorrhea

R

Riphah International University

Status

Completed

Conditions

Primary Dysmenorrhea

Treatments

Other: KegelExercise
Other: 4-7-8 breathing technique

Study type

Interventional

Funder types

Other

Identifiers

NCT06339918
REC/RCR & AHS/23/0570

Details and patient eligibility

About

A randomized clinical trial will be conducted at Riphah International University QIE Campus in Lahore, using non-probability convenience sampling with 28 participants. Criteria include women aged 14-26, nulliparous, experiencing primary dysmenorrhea, with normal menstrual cycles and the ability to exercise independently. Group A will receive kegel exercises and 4-7-8 breathing techniques over 8 weeks, while Group B will only receive the breathing technique. Assessments will be done on menstrual cycle days, with follow-ups at weeks 4 and 8 using specific scales. Data will be analyzed using SPSS version 27.

Full description

This study will be a randomized clinical trial. Riphah International University QIE Campus in Lahore will serve as the site of data collecting and intervention services. Non-probability convenience sampling will be the method of sampling. The study's sample size will be 28 participants. Inclusion criteria for this study will be: women between ages 14-26 years, nulliparous women, with a score greater than 4 in WALIDD primary dysmenorrhea intensity scales, history of normal menstrual cycles that lasts 3-7 days and ranged from 21- 35 days, ability to perform exercises independently. Group A will be given kegel exercises as well as 4-7-8 breathing techniques for a total of 8 weeks with 4 sessions per week. Whereas, group B will be given the 4-7-8 breathing technique only. Initial assessment will be taken on the 3rd day of menstrual period. Follow-up assessment will be taken after week 4 post interventions and final assessment will be done after week 8 post intervention. WaLIDD primary dysmenorrhea intensity scale, Pain Self-Efficacy Questionnaire (PESQ), and Numeric Pain Rating Scale (NPRS) will be the data collecting instruments.

Enrollment

28 patients

Sex

Female

Ages

14 to 26 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Nulliparous women
  • Women with a score greater than 4 on WALIDD primary dysmenorrhea intensity scale
  • Women having a history of normal menstrual cycles that lasts 3-7 days and range from 21- 35 days.
  • Ability to perform exercises independently

Exclusion criteria

  • Women with very mild primary dysmenorrhea
  • Women treated for ovarian cysts or other gynecological issues
  • Women currently taking medication for dysmenorrhea
  • History of any systemic illness
  • A history of psychological conditions that could influence the perception of pain and functional activity.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

28 participants in 2 patient groups

Kegel Exercise with4-7-8 Breathing technique group:
Experimental group
Description:
GroupAwill be given the intervention of kegel exercises as well as 4-7-8 breathing techniques for about 15 minutes per session for a total of 8 weeks with 4 sessions per week. To perform kegel exercises, tighten pelvic floor muscles like trying to hold in urine and stool. 4-7-8 breathing Technique can be performed by telling the participant to inhale to the count of 4. Hold their breath for 7 counts. To the count of 8, release air via their mouth.
Treatment:
Other: 4-7-8 breathing technique
Other: KegelExercise
4-7-8 Breathing Technique group
Active Comparator group
Description:
In this group, we only perform the 4-7-8 Breathing Technique by telling the participant to inhale to the count of 4. Hold their breath for 7 counts. To the count of 8, release air via their mouth.
Treatment:
Other: 4-7-8 breathing technique

Trial contacts and locations

1

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Central trial contact

ghulam Fatima, PhD*

Data sourced from clinicaltrials.gov

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