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The Efficacy of Theta-Binaural Beat Stimulation Combined with Music Medicine for Chronic Low Back Pain Management

The Efficacy of Theta-Binaural Beat Stimulation Combined with Music Medicine for Chronic Low Back Pain Management

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260109001
Enrollment
126
Registered
2026-01-09
Start date
2024-01-02
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Chronic low back pain (CLBP) Binaural beats, chronic low back pain, music therapy, non-pharmacological treatment, pain management.

Interventions

Listen to binaural beat combined with acoustic music for 20 minutes daily for 14 days.,Listen to acoustic music for 20 minutes daily for 14 days.,Continue current therapy without listening to the musi
Binaural beat combined with acoustic music,Acoustic music ,Conventional therapy

Sponsors

Associate Prof. Nuj Tontisirin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Adults aged 18 years or older 2) Chronic moderate to severe low back pain (i.e., average pain intensity in the past week more than or equal 4/10) persisting for more than three months. 3) Participants were recruited from pain clinics at Ramathibodi Hospital, King Chulalongkorn Memorial Hospital, Phramongkutklao Hospital, Songklanagarind Hospital, Siriraj Hospital, Maharaj Nakorn Chiang Mai Hospital, and Srinagarind Hospital.

Exclusion criteria

Exclusion criteria: Exclusion criteria included 1) Diagnosed neurological or psychiatric disorders 2) Clinically significant anxiety or depression (T-score more than or equal to 60 on the Patient-Reported Outcomes Measurement Information System-29 (PROMIS-29)-Anxiety and Depression scales) 3) Hearing impairment assessed via the whispered voice test 4) Illiteracy or inability to complete study documentation 5) Previous surgical or interventional procedures for CLBP within three months 6) Individuals with clinically significant anxiety or depression were excluded to minimize the potential confounding effects of high levels of psychological dysfunction on the study outcomes.

Design outcomes

Primary

MeasureTime frame
Average pain intensity reduction 2 weeks after intervention Numerical rating scale

Secondary

MeasureTime frame
Worst pain intensity 2, 4 weeks Numerical rating scale,Average pain intensity 2, 4 weeks Numerical rating scale,Pain interference 2, 4 weeks after intervention the Patient-Reported Outcomes Measurement Information System-29 (PROMIS-29),Patient-reported improvement 2, 4 weeks after intervention Patient Global Impression of Change (PGIC),Satisfaction 2, 4 weeks after intervention Satisfaction score 1-5 (1; Very unsatisfied- 5;Very satisfied)

Countries

Thailand

Contacts

Public ContactNuj Tontisirin

Faculty of Medicine Ramathibodi Hosptial

doctornuj@gmail.com022011513

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026