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Exercise intervention using behavior change techniques for low back pain in heavy manual workers: an exploratory study

Effects of a Behavior Change Techniques-Based Exercise Intervention Among Heavy Manual Workers with Low Back Pain: An Exploratory Study - Effects of a Behavior Change Techniques-Based Exercise Intervention Among Heavy Manual Workers with Low Back Pain: An Exploratory Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059670
Enrollment
60
Registered
2025-12-15
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Low back pain

Interventions

The initial intervention will be conducted within two weeks of registration. The intervention will last 12 weeks and will be delivered in a group format by a certified physical therapist in person. Th

Sponsors

Shimane University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Individuals experiencing lower back pain for over one month. 2. Individuals aged 20 to 60 years old. 3. Individuals engaged in heavy labor such as manufacturing, whose primary work duties do not involve desk work. 4. Individuals not currently receiving rehabilitation programs or hospital treatment for back pain at the time of registration. 5. Individuals who fully understand the study content and can provide written consent.

Exclusion criteria

Exclusion criteria: 1. Individuals with a confirmed history of spinal disorders such as herniated discs, spinal stenosis, spinal compression fractures, spinal tumors, or infectious spondylitis. 2. Individuals currently restricted by a physician from exercise or physical activity due to low back pain or other health reasons. 3. Pregnant individuals or those who have undergone lumbar surgery within the past year. 4. Individuals with serious complications such as heart disease, respiratory disease, kidney disease, or liver disease, where participation in the study is deemed to potentially compromise safety. 5. Individuals with severe mental disorders (e.g., schizophrenia, major depressive disorder) that may make cooperation with or understanding of the study difficult. 6. Individuals who have difficulty communicating in Japanese. 7. Individuals deemed unsuitable for participation in this study by the research staff for other reasons.

Design outcomes

Primary

MeasureTime frame
Pain intensity (Visual Analog Scale) will be assessed using a questionnaire before and after the 12-week intervention period.

Secondary

MeasureTime frame
Before and after the 12-week intervention period, the following will be assessed using questionnaires: - Degree of ADL impairment (Roland-Morris Disability Scale) - Presenteeism (The Quantity and Quality method) - Pain catastrophizing (Pain Catastrophizing Scale) - Kinesiophobia (Tampa Scale for Kinesiophobia) - Self-efficacy - Stages of change Physical activity levels will be assessed using an activity monitor.

Countries

Japan

Contacts

Public ContactTakehiko Tsujimoto

Shimane University Faculty of Human Sciences

tsujimoto@hmn.shimane-u.ac.jp+81-852-32-9060

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026