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EFFECTS OF ADDING THE FLOSSING TECHNIQUE TO CORE STABILIZATION EXERCISE ON MUSCLE THICKNESS, FUNCTIONAL CAPACITY, PAIN, AND DISABILITY IN INDIVIDUALS WITH CHRONIC NON-SPECIFIC LOW BACK PAIN: A RANDOMIZED CONTROLLED TRIAL

EFFECTS OF ADDING THE FLOSSING TECHNIQUE TO CORE STABILIZATION EXERCISE ON MUSCLE THICKNESS, FUNCTIONAL CAPACITY, PAIN, AND DISABILITY IN INDIVIDUALS WITH CHRONIC NON-SPECIFIC LOW BACK PAIN: A RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220523002
Enrollment
45
Registered
2022-05-23
Start date
2021-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Chronic non-specific low back pain Chronic non-specific low back pain, flossing technique with core stabilization exercise

Interventions

The participants will perform core stabilization exercises with the floss band wrapped around the trunk area for three sets of 4 exercises (curl-up, side plank, alternative arm-leg extension in quadru
Flossing technique with corestabilization exercise,Core stabilization exercise,Control

Sponsors

Faculty of Physical Therapy, Mahidol University, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Body mass index (BMI) between 18.5 and 24.9 kg/m2 2. Abdominal skin fold less than 27.8 mm for men and 33.8 mm for women 3. Have a low back pain episode of longer than 3 months with mild to moderate pain average pain (in the past week) (VAS scores 1 to 64 mm) 4. Untrained of any core stabilization within a year

Exclusion criteria

Exclusion criteria: 1. Having severe pain or inflammation sign in the current episode 2. Having abdominal pain or other areas that might affect the intervention 3. Having any open wounds or skin diseases or burns in the back or abdominal area 4. Having rubber allergies 5. Having underlying diseases such as hypertension, diabetes, heart disease, vascular disease, arterial stenosis, abdominal aorta aneurysm, thrombosis, acute venous disorder, varicose vein, unstable medical conditions, tumor, cancer, metabolic syndrome, and any other unstable diseases diagnosed by a physician 6. Having a history of HNP, pain or referred pain from trunk to lower extremities, and fracture in a year 7. Having neurological diseases such as stroke, multiple sclerosis, and deficits of peripheral sensation 8. Having scoliosis, spondylolisthesis, spondylolisthesis, and lumbar structural instability 9. Fever or other infection that affects the intervention 10. Female participants on their menstrual period 11. Having prolonged use of corticosteroids for three months, antiplatelets, muscle relaxants, or NSAIDs within 72 hours, or any medications that relate to the change of muscle and blood circulation responses.

Design outcomes

Primary

MeasureTime frame
Muscle thickness Pre, Mid (3 week), Post (6 week) intervention Using the ultrasonography to measure the trunk muscle thickness, including Transversus abdominis, External abdominal oblique, Internal abdominal oblique, Erector spinae, Lumbar multifidus muscles

Secondary

MeasureTime frame
Pain intensity Pre, Mid (3 week), Post (6 week) intervention Using visual analog scale to detect pain at rest and aggravate,Oswestry Disability index Pre, Mid (3 week), Post (6 week) intervention Using Oswestry Disability Questionnaire in Thai version,2 minutes step test Pre, Mid (3 week), Post (6 week) intervention Ask the participants to stepping continuously for 2 minutes and counting the steps,5 times sit to stand Pre, Mid (3 week), Post (6 week) intervention Ask the participants to perform sit to stand continuously for 5 time and counting the time

Countries

Thailand

Contacts

Public ContactChattrarerk Wongcharoen

Faculty of Physical Therapy, Mahidol University

kp2609@hotmail.com0819624570

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026