Effect of Lumbar Proprioception Training on Primary Dysmenorrhea

Cairo University30 enrolled

Overview

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

Although previous studies reported the effect of physiotherapy practices through therapeutic exercises on primary dysmenorrhea as core muscles strengthening, core stability exercises, connective tissue massage and classical massage, relaxation, strengthening, stretching, aerobic exercises, pelvic floor muscle strengthening exercises, yoga and Pilates. None of them have investigated the effect of lumbar proprioception training on primary dysmenorrhea. Therefore, this study will be the first one which aims to investigate the effect of lumbar proprioception training on primary dysmenorrhea. This trial will include 2 groups; group A composed of 20 females that will receive hot packs and pelvic rocking exercises for 4 weeks and group B also composed of 20 females that will receive hot packs and pelvic rocking exercises in addition to lumbar proprioception training for 4 weeks.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Primary Dysmenorrhea

Interventions

lumbar proprioception trainingOTHER

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.

Hot packsOTHER

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

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 22 Years

Medical Language ↔ Plain English

Inclusion Criteria: * All females will have moderate to severe primary dysmenorrhea (as determined by WaLIDD Scale). * Their ages will range from 18 to 22 years old. * All females will be virginal and non-smokers. * Their BMI will be range from 20-25 kg/m2 * They have regular menstrual cycle with menstrual cycle length of 28-30 days. * They have persistent primary dysmenorrhea of more than 6 months Exclusion Criteria: * They shouldn't have musculoskeletal or neurological disorders, chronic LBP or sacroiliac dysfunction, diabetes, pelvic pathology or any gynecological disease. * They shouldn't experience a stressful event in the last 6 month. * Attending regular exercise training in the last 6 months. * Taking medications or vitamin and mineral supplements due to other medical conditions.

Locations (1)

Doaa Osman

Giza, Egypt

Outcomes

Primary Outcomes

Measurement of lumbar proprioception

It will be evaluated through Biodex system in both groups before and after treatment program through measuring the lumbar repositioning accuracy.

Time frame: 4 weeks

Secondary Outcomes

Calculation of score of WaLIDD Scale

It will be used to identify dysmenorrhea severity in both groups before and after treatment program through measuring combination of manifestations: subjective (intensity/Wong-Baker, work ability) and objective (days of pain, location) for both groups.The total score of 0 indicates without dysmenorrhea; 1-4 indicates mild dysmenorrhea, 5-7 indicates moderate dysmenorrhea, 8-12 indicates severe dysmenorrhea (Teherán et al., 2018).

Time frame: 4 weeks

lumbar curvature angle

it will be measured by Flexible ruler which is affected by the tilt of the pelvis, in both groups before and after treatment program.

Time frame: 4 weeks

Data from ClinicalTrials.gov

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