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Belt Squat Training for Non-Specific Low Back Pain

Belt Squat Training for Individuals with Chronic Non-Specific Low Back Pain - a Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06594731
Enrollment
25
Registered
2024-09-19
Start date
2024-03-01
Completion date
2024-06-30
Last updated
2024-09-19

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

Conditions

Low Back Pain

Keywords

Feasibility study

Brief summary

The purpose of this project is to investigate the feasibility of using belt squat as an exercise intervention for people with chronic low back pain. We will recruit people with chronic low back pain as well as asymptomatic controls

Detailed description

The purpose of the current project is to evaluate the feasibility of performing belt squats in healthy participants and persistent non-specific low back pain (LBP) patients. For this project we wish to recruit 20 healthy volunteers 20 volunteers LBP patients through notices at Aalborg University, on www.forsog.dk, and on Facebook. The following inclusion and exclusion criteria will be used for the healthy subjects: Healthy men and women, age 18-60. And for the LBP patients: Non-specific LBP for more than twelve weeks without major sciatica (back pain >leg pain), age 18-60. Exclusion criteria pertinent to all subjects were: Leg pain greater than back pain, neuromuscular disorders, spinal or lower extremity fractures, infections, cancer, osteoporosis, dementia, BMI>35, current substance abuse, former lumbar surgery, persistent pain syndromes other than back pain, inflammatory rheumatic diseases. In the study, participants will perform hip belt squat training twice per week for 6 weeks. To test the feasibility of performing hip belt squat training in healthy participants and persistent LBP patients the project will be based on the Bowen feasibility model. This model lists eight different focus areas for feasibility studies, where this particular sub-project will focus on four of these areas being: acceptability, demand, implementation, and practicality. To test the acceptability and demand, subjects will be interviewed on their satisfaction, intention to continue use, actual use, perceived appropriateness, and perceived demand of the training. Implementation and practicality will be assessed by evaluation of the degree of execution, success or failure of execution, factors affecting implementation ease or difficulty, positive/negative effects on participants, ability of participants to carry out the training activities and a cost analysis. Lastly, to test the acceptance of methods relevant to the training, measures on lumbar flexibility, muscle strength, muscle mass (DEXA scan), pain sensitivity (pressure-pain threshold, PPT) using a handheld pressure algometer (Somedic, Sweden), muscle activity (Electromyographic measurement, EMG) and the following questionnaires: Fear-avoidance Beliefs Questionnaire (FABQ), Oswestry Disability Index (ODI) (which ranges from 0 (no disability) to 100 (bedridden)), health-related quality of life as measured by EuroQOL-5D (EQ-5D) (ranging from -0.596 to 1, with higher scores indicating better quality of life) will be carried out

Interventions

OTHERHip belt squat training

Hip belt squat training performed twice per week for 6 weeks

Sponsors

Aalborg University Hospital
CollaboratorOTHER
Mathias Kristiansen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy men and women * Men and women with non-specific low back pain for more than twelve weeks

Exclusion criteria

* Leg pain greater than back pain * Neuromuscular disorders * Spinal or lower extremity fractures * Infections * Cancer * Osteoporosis * Dementia * Current substance abuse * Former lumbar surgery * Persistent pain syndromes other than back pain * Inflammatory rheumatic diseases

Design outcomes

Primary

MeasureTime frameDescription
AcceptabilityImmediately after the interventionAcceptability of the intervention will be assessed using a 5 point likert scale ranging from completely agree to completely disagree on whether the intervention was acceptable or not.
DemandImmediately after the interventionDemand of the intervention will be assessed using a 5 point likert scale ranging from completely agree to completely disagree on whether the participants wish to incorporate belt squats into their future training.
ImplementationImmediately after the interventionImplementation of the intervention will be assessed using a 5 point likert scale ranging from completely agree to completely disagree on whether the intervention was feasible or not.
PracticalityImmediately after the interventionPracticality will be assessed by evaluation of the adherence level, computed as the percentage of completed training sessions.

Secondary

MeasureTime frameDescription
Oswetry Disability indexAssessed at baseline and immediately after the intervention periodA questionnaire measuring the degree of disability, which ranges from 0 (no disability) to 100 (bedridden).
Health related quality of lifeAssessed at baseline and immediately after the intervention periodA questionnaire measuring the easured health-related quality of life (EuroQOL-5D), ranging from -0.596 to 1, with higher scores indicating better quality of life.
Muscle strengthAssessed at baseline and immediately after the intervention periodMuscle strength was assessed in the hop belt squat exercise using a 5 repetition maximum test
Body compositionAssessed at baseline and immediately after the intervention periodTo assess changes in body composition a DEXA scan was performed. This test quantified lean body mass (kg) and fat mass (kg).
Fear-avoidance Beliefs QuestionnaireAssessed at baseline and immediately after the intervention periodFear-avoidance Beliefs Questionnaire (FABQ) measuring the amount of kinesiophobia, ranging from 0-96 with higher scores indicating higher levels of fear avoidance belief.
Lumbar flexibilityAssessed at baseline and immediately after the intervention periodLumbar flexibility was assessed using a custom made test.
Pain sensitivityAssessed at baseline and immediately after the intervention periodPressure-pain threshold was assessed using a handheld pressure algometer.
Muscle activityAssessed at baseline and immediately after the intervention periodElectromyography was used to assess muscle activation.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026