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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05848479
Other study ID # P.T.REC/012/004341
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 26, 2023
Est. completion date July 26, 2023

Study information

Verified date May 2023
Source Cairo University
Contact Eman M Mahmoud
Phone + 2 1091403074
Email amira.mahmoud2021@outlook.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will be conducted on 44 females with postpartum LBP & pelvic instability, selected from Dar of women hospital in port said to investigate effect of clamshell exercise on lumbo-pelvic stability and low back pain in postpartum women.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 44
Est. completion date July 26, 2023
Est. primary completion date July 26, 2023
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 35 Years
Eligibility Inclusion Criteria: 1. Post-partum females complaining of LBP and lumber instability 2. Their age will be ranged from 25-35 years. 3. Their BMI will be ranged from 25-30 kg/m2 Exclusion Criteria: 1. Spinal deformity. 2. Lower limb deformity. 3. Osteosarcoma 4. Mental disorders. 5-25>BMI>30 6-Performing any physical exercise at the time of the study. 7-Bad general Health

Study Design


Intervention

Other:
Abdominal bracing
they will perform 3 times/week of static abdominal contraction for six weeks.
clamshell exercise
Each women will be positioned in side lying on the floor, with the pelvis and the spine in neutral position, the hips will bent at 45° and the knees flexed to 90°. She will abduct the top knee as far as possible, while keeping the heels together, then return to the starting position , the position will be maintained for 5 seconds in an abduction state, and repeated 10 times, with rest for 1 minute to minimize muscle fatigue,they will perform 3 times/week fo 6 weeks

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Eman Mahmoud Mahmoud El-sayed Ellily

Outcome

Type Measure Description Time frame Safety issue
Primary Change in the degree of lumbopelvic instability Change in the degree of lumbopelvic instability will be measured by specific tests(The dip test, the runner pose test and the single leg squat test) and the pateint performance will be graded as poor or good change in the lumbopelvic instability degree will be measured at baseline and after 6 weeks of the interventions
Primary lumbopelvic range of motion Degree of lumbopelvic range of motion will be measured by goniometer change in the lumbopelvic instability degree will be measured at baseline and after 6 weeks of the interventions
Secondary severity of pain intensity change in low back pain intensity will be measured using visual analogue scale(VAS)
low back pain intensity
change in the lumbopelvic instability will be measured at baseline and after 6 weeks of the interventions
Secondary the degree of function disability the change in the degree of function disability will be measured by Oswestry disability index (ODI) change in the lumbopelvic instability will be measured at baseline and after 6 weeks of the interventions
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03515239 - Comparative Study Between Unillateral and Bilateral Lumbopelvic Fixation for Spinopelvic Dissociation