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Effect of Lumbar Proprioception Training on Primary Dysmenorrhea

NCT06051435 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-04-22

No results posted yet for this study

Summary

the aim of this study will be to investigate the effect of lumbar proprioception training on primary dysmenorrhea.

Conditions

  • Primary Dysmenorrhea

Interventions

OTHER

lumbar proprioception training

a) Sensorimotor training: Sensorimotor training and reconditioning of proprioceptive senses have recently been found to be helpful in increasing motor performance and coordination, muscle strength, sensorimotor abilities, increasing intermuscular control, and improving one's response to sensory information and muscle tone. Reconditioning of proprioceptive senses and sensorimotor training increases one's muscle adjustment ability, maximizes the sensory input in different parts of the body and aids in improving one's motor adjustment ability (Hwang et al ., 2013). Position Exercise methods as Hollowing exercise: Participants will be asked to contract the abdominal muscles, raising the center of movement toward the navel in a quadruped position.

OTHER

Hot packs

hot application in the form of hot packs on the lower abdomen and lower back for a total duration of 30 minutes, once per day, during the first two days of menstruation

OTHER

Pelvic rocking exercise

Pelvic rocking exercise

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Amel Mohamed Yousef, PhD · Professor, Cairo university

  • Hamada Ahmed Hamada, PhD · Assistant Professor, Cairo university

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
22 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-01
Primary Completion
2024-06-01
Completion
2024-06-30

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06051435 on ClinicalTrials.gov