Actively Recruiting

Phase Not Applicable
Age: 20Years - 45Years
FEMALE
Healthy Volunteers
NCT07419399

Acute Effects of Radiofrequency Diathermy in Postpartum Women With Diastasis Abdominis

Led by University of Valencia · Updated on 2026-02-19

48

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This clinical trial aims to compare the immediate tissue response in postpartum women with and without rectus abdominis diastasis (RAD) after undergoing radiofrequency diathermy (RFD) treatment. The main question it seeks to answer is: Do postpartum women with and without RAD exhibit different acute tissue responses in terms of pressure pain threshold, superficial thermal sensitivity, and tissue elasticity? To determine whether there are differences in these acute tissue responses between the groups, researchers will compare RFD with a sham RFD intervention in postpartum women with and without RAD. Participants will receive one session of either RFD or a sham RFD intervention and will complete three assessments: one at baseline and two after the intervention, one immediately afterwards and one 20 minutes afterwards.

CONDITIONS

Official Title

Acute Effects of Radiofrequency Diathermy in Postpartum Women With Diastasis Abdominis

Who Can Participate

Age: 20Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 20 and 45 years old
  • Body mass index (BMI) between 18.5 and 29.9 kg/m²
  • Postpartum period between 6 months and 1 year
  • For women with RAD, pathological RAD defined as inter-rectus distance greater than 2.2 cm (measured 3 cm above the navel)
Not Eligible

You will not qualify if you...

  • Previous surgeries involving the abdominal wall
  • Cesarean deliveries
  • Women diagnosed with chronic pain

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Physiotherapy. University of Valencia

Valencia, Valencia, Spain, 46022

Actively Recruiting

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Research Team

M

Marta Inglés de la Torre, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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