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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06280989
Other study ID # P.T.REC/012/004768
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 15, 2024
Est. completion date August 2024

Study information

Verified date February 2024
Source Cairo University
Contact Hala ma Morsy, Bachelor
Phone 0020-01028616865
Email halamohamed8.11.2018@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the aim of this study is to investigate the efficacy of kinesio taping versus myofascial release technique on menstrual low back pain in young females


Description:

: Menstrual low back pain is a prevalent condition among women. Menstrual low back pain occurrence is affected by hormonal changes. Menstrual low back pain incidence more than 40% to 50% during the menstrual phase (days 1-6) of the menstrual cycle, while the range of prevalence was 45 to 95%. It has a high prevalence among females, especially females aged 20 to 25 years old. Hormonal changes might play an important role in the formation of Menstrual low back pain and is the main cause of feeling of pain during menstrual cycle. kinesio taping and myofascial release technique play an important role in the treatment of Menstrual low back pain. this trial has two groups; one will receive kinesio taping three days and the second will receive myofascial release technique for12 sessions through 3 consecutive menstrual cycle


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 44
Est. completion date August 2024
Est. primary completion date July 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: 1. Healthy young virgin females suffering from menstrual low back pain diagnosed by the gynecologist. 2. Their ages will be ranged from 18-25 years' old 3. Their body mass index will be ranged from 20-25 kg/m2. 4. All females have regular menstruation 5. Their pain intensity is scored as > 4 on VAS just before or during the first 3 days of the menstruation - Exclusion Criteria: Females will be excluded from the study if they have: 1. Any orthopedic problems such as trauma at lower spine, congenital malformation at spine and scoliosis. 2. Any gynecological problem such as irregular menstrual cycle, secondary dysmenorrhea due to endometriosis, ovarian cyst, uterine fibroid and congenital malformation or pelvic inflammation. 3. Athletic females 4. Allergy to kinesio taping. -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
kinesio taping
Before treatment, all female participants will undergo an allergic test on the anterior surface of the elbow. To ensure cleanliness, alcohol will be used to clean the areas to be evaluated before applying the tape. The H technique will be employed to apply KT over the lumbar region. Participants will be instructed to bend forwards from the waist, and two vertical strips will be applied. These strips will stretch the Golgi tendon organ on both sides of the spine from the top of the buttock cleft upwards to a mid-point, with less than 25% stretch . Additionally, a horizontal strip will be attached across the left and right sacroiliac joints. This strip will be stretched to 50% of its maximum capacity,.
myofascial release technique
myofascial release technique will be applied from prone on lumbar paravertebral muscles by using the olecranon of the physical therapist for 3 minutes, thoracolumbar fascia by using cross-handed hold, with hands placed on the T12-L1 levels and on the sacrum for 5 minutes without repetition and quadratus lumborum by using elbow with low pressure obliquely towards the center of the column for 7 min. Additionally, from supine on psoas muscle by transversal sliding of the psoas fascia. The therapist will place the hands laterally 3 cm from the umbilicus.

Locations

Country Name City State
Egypt Hala mohamed ahmed morsy Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain intensity The scale that will be used the VAS ;each subject will instructed to put point on line from no pain to tolerable pain up to four weeks]
Primary pain pressure threshold will be measured by pressure algometer up to four weeks]
Secondary severity of dysmenorrhea will be measured by WaLIDD scale(intensity /Wong-Baker, work ability , days of pain and location). Where (0) without dysmenorrhea, (1-4) mild dysmenorrhea, (5-7) moderate dysmenorrhea, (8-12) sever dysmenorrh up to four weeks]
Secondary Assess the function disability level will be assess by Oswestry Disability Index (ODI). up to four weeks]
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