Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05751694

Effectiveness of Visceral Manual Therapy in Bruxist Patients

Led by University of Seville · Updated on 2025-02-26

68

Participants Needed

1

Research Sites

156 weeks

Total Duration

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AI-Summary

What this Trial Is About

Objective: check the effectiveness of visceral manual therapy on bruxist patients Design: Experimental, analytical, longitudinal, prospective, randomized, single-blind study with a blinded evaluator. Subjects: 68 subjects over 18 years old, with bruxism (diagnoses by a dentist). Methods: Subjects will be randomized into 2 groups: an experimental group (EG) to which a visceral manual technique will be applied and a control group (CG) to which a placebo manual technique will be administered. Both groups will receive 2 interventions one week apart. The measurements will be made before and after the interventions, and a last measurement will be made one month after the last intervention. Therefore, the patient will visit the center 3 times.

CONDITIONS

Official Title

Effectiveness of Visceral Manual Therapy in Bruxist Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects with bruxism diagnosed and referred by a dentist
  • Age older than 18 years
Not Eligible

You will not qualify if you...

  • Recent craniofacial, mandibular, or cervical trauma or fracture
  • Temporomandibular joint surgery
  • Acute pain from other dental issues like caries or dental root inflammation
  • History of abdominal surgery
  • Gastric ulcers
  • Gastritis
  • Previous or current gastric cancer
  • Neurological or systemic diseases
  • Pregnancy or breastfeeding
  • Receiving chemotherapy or radiotherapy
  • Cognitive, psychosomatic, or psychiatric illnesses affecting data
  • Rheumatic systemic diseases such as arthritis, osteoarthritis, gout, or psoriasis
  • Cerebrovascular or brain diseases
  • Arrhythmia or other heart problems
  • Implanted electronic devices
  • Drug or alcohol abuse, or use of medications affecting the central nervous system like antidepressants, anxiolytics, or anticonvulsants
  • Previous experience with manual treatment of the diaphragm

AI-Screening

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Trial Site Locations

Total: 1 location

1

Nursing, Physiotherapy and Podiatry Faculty

Seville, Spain, Spain, 41009

Actively Recruiting

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Research Team

L

Lourdes M Fernández Seguín, PhD

CONTACT

C

Cayetano Navarro Rico, Phd Student

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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