Effect of Capacitive and Resistive Radiofrequency on Postpartum Diastasis Recti

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-35
SponsorCairo University

About this trial

To evaluate the effect of capacitive and resistive radiofrequency on postpartum rectus abdominis diastasis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

1. Postpartum women (7 days after delivery) having diastasis recti (separation between the two recti more than 2.5cm at the level of umbilicus).

Disqualifiers

Abdominal or back surgery.

Abdominal hernia.

History of abnormal pregnancy, uterine fibroid or polyhydramnios during pregnancy.

Neurological disorders as multiple sclerosis, stroke and spinal lesion.

Trial design

Design model

Parallel

Treatments tested in this trial

  • abdominal belt

    Device

    40 postpartum women will only wear abdominal belt for 14 weeks.

  • TECAR therapy

    Device

    will wear the same abdominal belt for 6 weeks then participating in TECAR therapy 3 sessions /week for 8 weeks.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: control groupActive comparator 1 intervention
Group B: study groupActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Ultrasound

The distance between the recti muscles at 3 levels will be measured at the beginning and again at the end of the study duration, i.e., 8 weeks. The desired measurement locations will be marked with a water-soluble pen: 4.5 cm above the umbilicus, at the midpoint, and 4.5 cm below the umbilicus. The measurements will be performed at rest and during contraction. Each woman will be asked to lie in a crock lying position, crossing the arms over the chest and raising the head until the spine of the scapulae will be off the table surface. The women will maintain a partial curl-up while the examiner palpates the medial borders of the right and left rectus abdominis muscle bellies at the marked location. With the linear transducer, it will be positioned transversely along the linea alba in the direction of the muscles and adjusted to perceived inert recti distance width. Three trials will be taken for each assessment, and the mean will be recorded. (Khandale \& Hande, 2016).

Time frame
14 week
2

trunk flexors strength and endurance

Trunk flexion strength will be graded from zero to five using Daniels and Worthingham's procedure (Hislop et al., 2013) as follows: Grades: (Hislop et al., 2013). Grade 5 (Normal) Patient complete ROM until inferior angle of the scapulae are off table (weight of arms serves as resistance). Grade 4 (Good) Patient complete ROM until inferior angle of the scapulae are off table. Resistance of arms is reduced in the cross-chest position. Grade 3 (Fair) Patient complete ROM and lifts trunk until inferior angle of the scapulae are off table with arms at side. Grade 2 (Poor) Patient is unable to clear the inferior angle of the scapula from the table Grade 1 (Trace) No depression of the rib cage but visible or palpable contraction occurs. Grade 0 (Zero) No activity Patient Positioning: Grade 5 (Normal): Supine with fingertips lightly touching the back of the head. For grade 4: Supine with arms crossed over chest. For grade 3: Supine with arms at side. For grade 0 to 2: Supine with arms at

Time frame
14 week
3

Assessment of functional status

All participating women with diastasis recti in both groups (A\&B) will be asked to fill the Inventory of functional status after childbirth questionnaire before and after the end of the study program.

Time frame
14 week

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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