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Effect of Ultrasound Cavitation on Static and Dynamic Balance in Obese Postnatal Women With Diastasis Recti

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Rectus Diastasis

Treatments

Other: low caloric diet regimen
Device: ultrasound cavitation

Study type

Interventional

Funder types

Other

Identifiers

NCT05900856
p. t.REC/012/003570

Details and patient eligibility

About

the aim of this study is to investigate the efficacy of ultrasound cavitation on static and dynamic balance in obese postnatal women with diastasis recti

Full description

Rectus diastasis defined as the widening of the linea alba by more than 2 cm at the midline. A great proportion of pregnant women are complaining from rectus diastasis during pregnancy reaching 100% of all women that may continue for years after delivery in 66% of women, and do not return to the first state automatically. This occurs due to a combination of physiologic, hormonal and mechanical factors, leading to reduction of abdominal muscle functional strength, increased low back pain out of increased lumbar hyperlordosis and postural instability, which may seriously disable woman from taking care of her baby, perform her daily activities. Weight gain is one of the predisposing factors that increases the possibility of developing rectus diastasis postpartum. Being obese increases liability to have rectus diastasis as carrying excess abdominal fats puts greater pressure against linea alba and can develop or aggravate symptoms for both men and women. This massively displaces the center of gravity anteriorly, disturbs body balance, increases joint loads and influences negatively pelvis posture leading to increased anterior pelvic tilt with subsequent exaggerated lumbar hyperlordosis. Ultrasound cavitation is the most revolutionary method that destroys excess body fat through creating microbubbles and releasing energy that breaks down fat cells. This trial has two groups: one will be treated by low caloric diet regimen only and the second one will be treated by ultrasound cavitation in addition to low caloric diet regimen for eight weeks

Enrollment

60 patients

Sex

Female

Ages

25 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. All women had a diastasis recti more than 2.5 cm and less than 4 cm in supra umbilical region.
  2. Their ages were ranged from 25: 35 years.
  3. Their BMI was more than 30 Kg/ m2.
  4. All women were with lumbar hyperlordosis.
  5. All women were multipara.
  6. Their mode of delivery was normal vaginal delivery.
  7. They were selected from 2: 5 months postnatal.

Exclusion criteria

  1. Previous cesarean section.
  2. Previous abdominal and/ or back operation.
  3. Spinal disorders.
  4. Abdominal skin diseases.
  5. Serious diseases such as heart disease, pace maker, uncontrolled diabetes or hypertension, autoimmune disease, malignancy, gastric ulcer, liver or renal failure and any other contraindication for body sculpting-weight loss.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

low caloric diet regimn
Experimental group
Description:
patients will follow low caloric diet regimn (1600: 2000 Kcal/ day), lipids approximately (20: 35%) of total caloric intake, protein approximately (10: 35%) of total caloric intake and high complexed carbohydrate intake approximately (45: 65%) of total caloric intake (with increased fiber-rich whole grain breads, cereals, fruits and vegetables), for eight weeks.
Treatment:
Other: low caloric diet regimen
ultrasound cavitation for 30 minutes, twice per week for eight weeks and low caloric diet regimn
Experimental group
Description:
ultrasound cavitation, Dae Yang, Mabel 6, frequency (50: 60) Hz, power consumption 150 W, power input AC (100: 230) V, hand probe diameter 8.0 cm, serial number DY73-15037, produced by DAEYANG MEDICAL company, made in Korea. the device will be applied for 30 minutes on the abdominal area, twice per week for eight weeks. low caloric diet regimn patients will follow low caloric diet regimn (1600: 2000 Kcal/ day), lipids approximately (20: 35%) of total caloric intake, protein approximately (10: 35%) of total caloric intake and high complexed carbohydrate intake approximately (45: 65%) of total caloric intake (with increased fiber-rich whole grain breads, cereals, fruits and vegetables), for eight weeks.
Treatment:
Device: ultrasound cavitation
Other: low caloric diet regimen

Trial contacts and locations

1

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Central trial contact

Asmaa zahran, lecturer

Data sourced from clinicaltrials.gov

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