Core stability exercise
OtherPatients will receive specific core stabilizing exercises, focusing on Pelvic floor muscles ,Gluteus maximus, Gluteus Medius, specific abdominal muscles , the lumbar multifidus, and Erector spinae.
NCT Number: NCT07292051
Purpose of the study :
The purpose of the current study is investigating the effect of Blood Flow Restriction Training technique on postpartum pelvic girdle pain.
Trial opening soon.
Get Notified20 year–35 year
Female
Interventional
Not applicable
This study is a randomized controlled trial. To fulfill its purpose, we have two groups; control group (A) and experimental group (B) are two matched postpartum pelvic girdle pain groups. While group (A) will receive a core stability exercise program, group (B) will receive core stability exercise program with blood flow restriction technique.
The primary outcome measure will be pelvic girdle pain intensity, while the secondary outcomes will include pelvic girdle-related disability, health-related quality of life, Kinesiophobia , global improvement and ASLR-RE angle.
Treatment duration will be eight weeks.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will receive specific core stabilizing exercises, focusing on Pelvic floor muscles ,Gluteus maximus, Gluteus Medius, specific abdominal muscles , the lumbar multifidus, and Erector spinae.
Patients will receive the same core stability exercise added to Blood Flow Restriction Technique
Time frame: Baseline , 8 weeks and 16 weeks
In this study, pain severity will be measured using the mean of three 11-point NRS questionnaires for least, usual, and current pain over the previous 2 weeks.
Time frame: Baseline , 8 weeks and 16 weeks
pelvic girdle-related disability, measured by pelvic girdle questionnaire (PGQ)
Time frame: Baseline , 8 weeks and 16 weeks
Health-related quality of life, measured by the Arabic version of European quality of life-Five-Dimension Five-Level Instrument (EQ-5d-5L)
Time frame: Baseline , 8 weeks and 16 weeks
Kinesiophobia measured by an Arabic Tampa scale
Time frame: Baseline , 8 weeks and 16 weeks
Global improvement measured by global rating of change (GROC) scale
Time frame: Baseline , 8 weeks and 16 weeks
ASLR-RE angle, measured by Image J
Contact information is provided by the study sponsor or research team.
Kafrelsheikh University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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