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"physiotherapy in chronic low back pain "effect of electroacupuncture in treatment of chronic low back pain

Evaluation and Comparison of the Effectiveness of electroacupuncture and conventional physiotherapy for pain management and functional improvement in patient with nonspecific chronic low back pain(NCLBP):A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191002044951N3
Enrollment
50
Registered
2025-06-11
Start date
2025-09-22
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

non specific chronic low back pain. Low back pain

Interventions

Intervention 1: Intervention group: Physiotherapy group (Group 1): Participants in this group will undergo 6 physiotherapy sessions twice a week by trained physiotherapists, and each session will incl

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Adults 18 to 65 years old The duration of symptoms should be at least 3 months Baseline pain intensity =4 on the Visual Analog Scale (VAS) Patients who are capable of providing informed consent

Exclusion criteria

Exclusion criteria: Previous lumbar spine surgery Patients with serious pathological disorders whose chronic back pain is caused by reasons such as spinal stenosis, spondylolisthesis, malignancy ,.... Pregnancy Patients who have contraindications for TENS Severe mental disorders Contraindications to electroacupuncture: Such as bleeding disorders or severe fear of needles and sensory disorders . Also, heart failure and a history of seizures are contraindications to electroacupuncture. Language barrier or cognitive impairment

Design outcomes

Primary

MeasureTime frame
Pain according to VAS and quality of life according to SF-36 Questionnaire. Timepoint: Outcomes are assessed at three time points: at baseline, three months, and six months after the intervention. Method of measurement: VAS score and SF-36 Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKourosh Mansory

Iran University of Medical Sciences

Mansoori.k@iums.ac.ir+98 21 3848 7000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026