Prevalence of Lower Cross Syndrome Among Female College Students and Its Relation With Dysmenorrhea

NCT06766955 | Not Yet Recruiting

• 1 other identifier: P.T.REC/012/005378
• Study Type: observational
• Target: 140
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of the study is to find out the prevalence of lower cross syndrome among female college students and its relation with dysmenorrhea.

Conditions

Cross Syndrome

Outcome Measures

Primary Outcomes (4)

• Measurement of iliopsoas muscle length

  The Thomas test is used to assess the hip flexion Tightness. Position: The measurement of iliopsoas muscle length involved the subject lying supine on a plinth with one thigh protruding while the examiner checks for excessive lordosis. The non-tested hip is flexed and held close to the chest to stabilize the pelvis and flatten the lumbar spine. Using a universal goniometer, the examiner measures the iliopsoas length on the opposite side. The fulcrum is placed above the greater trochanter, the movable arm parallel to the femoral shaft, and the stationary arm parallel to the plinth. If the hip flexion angle exceeds 15 degrees, the patient's straight leg rises off the table and a muscle stretch end feel will be felt, the iliopsoas is considered tight.

  6 weeks

• Measurement of length of spinal extensors muscle

  The length of the spinal extensor muscles will be measured by modified Schober test while a female college student standing and her back facing the examiner. A reference line is marked at the intersection of the Venus dimples (Posterior superior iliac spine PSIS) on her lower back, with additional lines drawn 10 cm above and 5 cm below this point. The student then bends forward, and the examiner measured the increase in distance between these points using a measuring tape. The outcome measure is calculated by determining the differences between these points

  6 weeks

• Measurement of strength of abdominal muscle

  In this procedure, females are placed in a supine position with different arm placements based on the grade. The examiner stands beside the table at the chest level to ensure the scapula clears the table. The patient is asked to assume the end position by flexing their trunks fully, curling up until the scapula is off the table. They were guided with the instruction, "Tuck your chin and lift your head, shoulders, and arms off the table, as if doing a sit-up and hold it." (Magee, 2002). The gradings of this test are: Normal 5= Hands behind neck, until scapulae clear table 20-30sec hold. Good 4= Arms crossed over chest, until scapulae clear table 15-20sec hold. Fair 3= Arms straight, until scapulae clear table 10-15 sec held. Poor 2= Arms extended, towards knees, until top of scapulae lift from table 1-10 sec hold. Trace 1= Unable to raise more than head off table.

  6 weeks

• Measurement of gluteus Maximus strength

  The subject is placed in prone with the hips straight and the knee flexed to 90 degrees. The student is asked to extend the hip, keeping the knee flexed. Anterior force is applied to the posterior thigh. The pelvis is stabilized during the movement. Both legs are tested. The grading of this test are: Normal 5 = indicates that the individual achieves complete hip extension and can maintain the end position against maximal resistance. Good 4 = signifies that hip extension is achievable and can be sustained against heavy to moderate resistance. Fair 3 = denotes the ability to complete full hip extension and maintain the end position, although no resistance is applied. Poor 2 = reflects the capacity to perform the full range of hip extension while in a side-lying position. Trace 1 = is characterized by palpable contractions of the gluteus maximus, which manifest as a narrowing of the gluteal crease, without any observable movement at the joint.

  6 weeks

Secondary Outcomes (1)

• Assessment of menstrual symptoms

  6 weeks

Study Arms (1)

female college students

140 Medical and Non-Medical Female students participated in this study. They were selected randomly from Cairo University and the British university in Egypt.

Eligibility Criteria

• Age: 18 Years - 25 Years
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

Medical and Non-Medical Female students participated in this study. They were selected randomly from Cairo University and private universities in Cairo.

You may qualify if:

• They were virgin, healthy female college students.
• They had regular menstruation (3-8 days in duration, with 21-35 days in-between).
• Their ages ranged from 18 to 25 years old.
• Their body mass index (BMI) will range from 18 to 24.9 Kg/m2.
• Their waist- hip ratio was less than (0.8).

You may not qualify if:

• History of back or lower limb surgery
• Trauma to back or lower extremity
• Rheumatoid arthritis
• Spinal deformity such as kyphosis and scoliosis.
• Any neurological disease
• Uncooperative volunteers.

Sponsors & Collaborators

• Cairo University: lead

Study Sites (1)

Farida Bakr Mohamed

Cairo, Egypt

Location

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type Preus

Study Officials

• Amir A Gabr, Professor

  Cairo University

  STUDY DIRECTOR

• Dalia M. Kamel, Professor

  Cairo University

  STUDY CHAIR

Central Study Contacts

Farida B Mohamed, Master

CONTACT

+201273059799; faridabakr2019@gmail.com

Amira Nagy, PHD

CONTACT

+201021177871; Amira.nagy@rochetmail.com

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal investigator

Study Record Dates

• First Submitted: January 4, 2025
• First Posted: January 9, 2025
• Study Start: January 10, 2025
• Primary Completion: February 25, 2025
• Study Completion: March 13, 2025
• Last Updated: January 9, 2025

Record last verified: 2025-01

Locations

EG (1)