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Feasibility of a Robotic Massage System in the Intervention for Chronic Nonspecific Low Back Pain: A Pilot Study Targeted at Healthcare Professionals.

Feasibility of Massage Robot in the Intervention of Chronic Nonspecific Low Back Pain: A Pilot Study for Healthcare Providers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001495
Enrollment
Unknown
Registered
2026-06-17
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Chronic nonspecific low back pain

Interventions

Massage Robot Intervention Group:EMMA Massage Robot

Sponsors

First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
23 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) On-duty medical staff with =1 year of work experience and occupational-related low back pain characteristics. (2) Meets domestic and international guidelines for diagnosis of NSLBP, with pain duration =12 weeks. (3) Pain intensity (VAS score) of 3-7 points (mild to moderate pain). (4) Able to independently complete activities of daily living (ADL), and willing to clinical observation and follow-up. (5) Signed written informed consent, voluntarily participating in the study and complying with the trial protocol.

Exclusion criteria

Exclusion criteria: (1) Clearly diagnosed with specific low back pain (e.g., intervertebral disc herniation with nerve root lesions, spinal tumors, fractures, infections, severe osteoporosis, etc.). (2) Have undergone lumbar spine surgery or other invasive procedures within the past 24 weeks, which may affect the assessment of this study. (3) Have acute severe comorbidities (e.g., cardiovascular or cerebrovascular events, severe hepatic or renal dysfunction) or mental/cognitive impairments, making it impossible to cooperate with the questionnaire assessment. (4) Pregnant or breastfeeding women. (5) Allergic to or showing obvious intolerance to the device materials (e.g., silicone end-effectors). (6) Have received frequent massage, physical therapy, or similar interventions within the past 12 weeks, or the investigator believes other reasons may interfere with the results of this trial. (7) Other situations deemed unsuitable for inclusion by the investigator, such as extremely poor compliance or inability to complete follow-up.

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Pain Threshold;ODI;SF-12;Patient Satisfaction;

Countries

China

Contacts

Public ContactZhang Wei

First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine

james399@126.com13820590796

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026