Immediate Effects of Myofascial Release on the Quadriceps or Hamstrings on Active Cervical Range of Motion

Healthy Clinical Trial

Official title:

Immediate Effects of Myofascial Release on the Quadriceps or Hamstrings on Active Cervical Flexion and Extension Range of Motion

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05725811
• Other study ID #: ESS/FSA-206/22-2
• Status: Completed
• Phase: N/A
• Start date: February 20, 2023
• Est. completion date: April 11, 2023

Study information

• Verified date: May 2023
• Source: University Fernando Pessoa
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to verify the immediate effects of quadriceps or hamstring myofascial release on the active cervical flexion and extension range of motion.

Description:

After completing the questionnaire, 60 healthy college students will be randomly divided into three groups named Intervention Group 1 (IG 1) (n=20), Intervention Group 2 (IG 2) (n=20) and Control Group (CG) (n=20). In the first assessment (M0), the cervical flexion and extension range of motion will be measured with a goniometer. The myofascial release technique (foam roller) will be applied on the hamstrings (IG 1) or quadriceps (IG 2) of the dominant lower limb for 4 minutes (3 series of 1 minute with 30s rest). Participants in the control group will remain at rest sitting in a chair for 4 minutes.

Immediately after the intervention/control, both groups will be assessed, again (M1).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: April 11, 2023
• Est. primary completion date: March 10, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 37 Years

Eligibility

Inclusion Criteria:

• Healthy university students of both genders with normal mobility of the joints.

Exclusion Criteria:

• Deformities in the lower quadrant region of the body;

• Complaints in this region in the last 6 months;

• Surgical procedures or musculoskeletal, cardiac, renal, metabolic, neurological and or oncological pathologies

• Pregnant women

• Ingestion of non-steroidal anti-inflammatory drugs or consumption of any type of narcotic drugs and participants who have drunk alcohol in the last 12 hours.

Related Conditions & MeSH terms

• Healthy

Intervention

Other:
• Dynamic foam rolling
The foam roller will be in contact with the muscle being tested and the patient will exert a load until they feel a slight pain. In this way, the patient performs a self-massage in the direction of the muscle fibers.

Locations

Country	Name	City	State
Portugal	Ricardo Cardoso	Porto
Portugal	Ricardo Cardoso	Porto

Sponsors (1)

Lead Sponsor	Collaborator
University Fernando Pessoa

Country where clinical trial is conducted

Portugal, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of active cervical range of motion in flexion and extension.	Data will be collected in two moments: baseline (M0) and after the intervention/control (M1). Participants will be asked to sit with their spine straight against the back of the chair. The ankles, knees and hips of the subjects will be positioned at right angles and the arms crossed over the chest to minimize thoracic movements.; The position of the goniometer (GIMA, 37.5 x 6.5 x 0.5 cm) will be as follows: the fixed point at the level of the external acoustic meatus, and the mobile arm at the level of the base of the nose (initial position: 90°). The fixed arm will be immobile, parallel to the ear and perpendicular to the ground. Prior to the test, each participant will have performed both movements until the final sensation is reached in order to increase the fluidity of the test. Thus, the first movement asked of the patient will be a flexion followed by an extension (the examiner will take the average of three measurements).	Change from Baseline (M0) to Immediately after intervention or control (M1)