Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
NCT06968026

High-Intensity, Low-Frequency Periodic rTMS Over the Right Dorsolateral Prefrontal Cortex on Cardiac Autonomic Regulation in Women With Recurrent Pregnancy Loss and Anxiety

Led by Shenyang Jinghua Hospital · Updated on 2026-04-21

55

Participants Needed

3

Research Sites

49 weeks

Total Duration

On this page

Sponsors

S

Shenyang Jinghua Hospital

Lead Sponsor

C

Central Hospital Affiliated to Shenyang Medical Collage

Collaborating Sponsor

AI-Summary

What this Trial Is About

This proof-of-concept trial investigates whether high-intensity, low-frequency repetitive transcranial magnetic stimulation (rTMS) targeting the right dorsolateral prefrontal cortex (DLPFC) can improve autonomic cardiac regulation in women with recurrent pregnancy loss (RPL) and anxiety. The study explores the lateralised function of the DLPFC in emotional and autonomic control and tests a novel neuromodulation-based strategy to relieve anxiety and sympathetic overactivation.

CONDITIONS

Official Title

High-Intensity, Low-Frequency Periodic rTMS Over the Right Dorsolateral Prefrontal Cortex on Cardiac Autonomic Regulation in Women With Recurrent Pregnancy Loss and Anxiety

Who Can Participate

Age: 18Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female, aged 18 to 45 years, and right-handed
  • Diagnosis of recurrent pregnancy loss with two or more consecutive miscarriages before 28 weeks of gestation
  • Currently not pregnant or presenting with a missed abortion confirmed by ultrasound
  • Hamilton Anxiety Rating Scale score of 14 or higher and Hamilton Depression Rating Scale score below 17
  • Confirmed diagnosis of at least one DSM-5 anxiety disorder subtype including generalized anxiety disorder, panic disorder, social anxiety disorder, or post-traumatic stress disorder based on a psychiatric interview
Not Eligible

You will not qualify if you...

  • Contraindications to transcranial magnetic stimulation such as metallic implants or history of epilepsy
  • Uncontrolled blood pressure with systolic above 180 mmHg or below 90 mmHg
  • Presence of major medical conditions including hyperthyroidism, atrial fibrillation, valvular heart disease, sinus bradycardia, neurological or cerebrovascular disorders, or chronic pulmonary disease
  • Clinically significant suicide risk
  • Current or past diagnosis of other psychiatric disorders including substance use disorders, schizophrenia, delusional disorder, psychotic disorders, bipolar disorder, or delirium

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

The Second Affiliated Hospital of Shenyang Medical College

Shenyang, Liaoning, China, 110001

Actively Recruiting

2

Shenyang Jinghua Hospital

Shenyang, Liaoning, China, China

Actively Recruiting

3

Central Hospital Affiliated to Shenyang Medical Collage

Shenyang, Liaoning, China

Actively Recruiting

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Research Team

Y

Yun-En Liu, MD

CONTACT

L

Lin Tao, MM

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

1

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