Effect of simultaneous use of thermal massage on muscle pain relief, cognitive function, concentration, stress, and fatigue improvement

A single-institution clinical trial to examine the effects of using a heat-massage device (CGM MB-1901) for improvement in muscle pain relief, cognitive function, concentration, stress, and fatigue for university students who have muscle pain and lead a sedentary life for a long time

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006885

Enrollment

Registered

2021-12-31

Start date

2021-07-05

Completion date

Unknown

Last updated

2022-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : 1. Clinical trial equipment: CGM MB-1901 2. Treatment: According to the randomized group, the following treatment was received for a total of 8 weeks. (2 times per day, 5 times per we

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Adult men and women who have muscle pain at neck or low back or shoulder. 2) Person who is recognized as suitable in screening tests 3) Person who can visit the hospital outpatient to participate in the study. 4) Person who voluntarily consents to this study. 5) Person who can follow directions well to instruction during the study.

Exclusion criteria

Exclusion criteria: 1) Patients with muscle pain due to disease in other organs (liver disease, cancer, rheumatic disease, thyroid disease, etc.) 2) Person who suspected of having myopathy, malignancy, spinal cord infection, thrombosis, etc. 3) Person with skin disease and hypersensitivity 4) Person who is at risk of deformity of the spine, vertebral fractures, and neurological abnormalities - Scoliosis of more than 20 degrees - History of severe osteoporosis and vertebral fractures due to osteoporosis 5) Person with spinal instability (Fail Back Syndrome) after previous spinal fixation surgery 6) Person with sensory impairment 7) Person who has had spinal surgery 8) Person who has received invasive spine treatment within 4 weeks before screening 9) Person with mental disorders that may affect participation in clinical trials or evaluation of symptoms 10) Patient who participated or will participate in the study that able to effects this study within 3 months. 11) Person diagnosed with osteoporosis 12) Pregnant or lactating woman 13) Any other person judged by the investigator that participation in clinical trials is inappropriate

Design outcomes

Primary

Measure	Time frame
Visual Analog Scale;Pain Disability Index	—

Secondary

Measure	Time frame
Electroencephalogram;Frankfurter Aufmerksamkeits-Inventar;Test-Anxiety Inventory;Global Assessment of Recent Stress;Academic Stress Test; Beck Depression Inventory - II ;Fatigue Severity Score	—

Countries

Korea, Republic of

Contacts

Public ContactKyung-Ah Yu

Presbyterian Medical Center

yka9504@hanmail.net+82-63-230-8857

Outcome results