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Masseter Muscle Stiffness After Heat Application and Percussion Therapy

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Enrolling

Conditions

Healthy Participants

Treatments

Device: massage gun
Device: heat treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT07237087
2025-00295

Details and patient eligibility

About

The purpose of this study is to evaluate the changes in the stiffness of the masseter muscle (a jaw muscle) before and after two types of treatment: applying commercial heat pads or using a commercial massage gun.

We will measure the muscle stiffness on the surface of the muscle using a special ultrasound probe, with a method called shear wave elastography.

When this muscle is too stiff, it's often linked to jaw pain and problems with the jaw joint - a condition known as Temporomandibular Disorder (TMD).

The goal is to find better treatment options for people with TMD and to collect data using this imaging technique.

Full description

In our study, participants will be randomly assigned to one of two groups. This is important to ensure reliable results and is called randomization.

The two groups are as follows:

Group A:

First, the stiffness of the masseter muscle in the cheek is measured using ultrasound. Then, we will assess the mouth opening, the muscle's sensitivity to pressure, bite force, and chewing efficiency using several short tests. After that, the masseter muscle will be treated with a massage gun with a soft attachment for 2 minutes. All tests will be repeated after the treatment.

Group B:

First, the stiffness of the masseter muscle in the cheek is measured using ultrasound. Then, we will assess the mouth opening, the muscle's sensitivity to pressure, bite force, and chewing efficiency using several short tests. After that, the masseter muscle will be treated with a heat pad for 20 minutes. The heat pad will be held in place with a strap, and participants may sit and read or relax during the treatment. All tests will be repeated after the treatment.

Each participant will receive both treatments (massage gun and heat pad), but in a different order depending on group assignment. There will be a two-week washout phase between the two treatments to ensure that the effects of the first treatment do not influence the second.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Willingness to participate to the study
  • Signed written informed consent

Exclusion criteria

  • Inability to follow procedures or insufficient knowledge of project language, inability to give consent
  • a history of drug ingestion within the past week (e.g. pain relievers, muscle relaxants, botox and anti-inflammatory drugs)
  • systemic diseases
  • Contraindications listed on the massage-gun instruction manual systemic and related to the use on the masseter area.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Group A: First massage gun, then heat treatment
Experimental group
Description:
The massage gun is the new treatment (experimental). Heat treatment is already commonly used for muscle stiffness and could be considered an active comparator. However, since its specific effects on the masseter muscle are not well established, it may also be classified as experimental.
Treatment:
Device: heat treatment
Device: massage gun
Group B: first heat treatment, then massage gun
Experimental group
Description:
The massage gun is the new treatment (experimental). Heat treatment is already commonly used for muscle stiffness and could be considered an active comparator. However, since its specific effects on the masseter muscle are not well established, it may also be classified as experimental.
Treatment:
Device: heat treatment
Device: massage gun

Trial contacts and locations

1

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Central trial contact

Nenad Lukic, Dr. med. Dr. med. dent.; Vera Colombo, PD Dr. sc. ETH

Data sourced from clinicaltrials.gov

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