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Efficacy of conventional physiotherapy and manipulative physiotherapy in the treatment of low back pain. A randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN47636118
Enrollment
440
Registered
2002-10-10
Start date
2000-01-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Low back pain Musculoskeletal Diseases Low back pain

Interventions

Subjects will be randomised into either the CPT or MPT groups: 1. CPT includes modalities such as heat and cold therapy, nerve stimulation, active exercises, hydrotherapy, etc. 2. MPT includes manual

Sponsors

Hong Kong Health Services Research Fund (Hong Kong)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients are medically referred 2. Patients presented no contraindication to Conventional physiotherapy (CPT) and Manipulative (MPT) physiotherapy 3. Aged 18 to 65 years 4. Low back pain (LBP) not treated by physiotherapist in the previous month 5. Duration of LBP at least 2 weeks before attending physiotherapy 6. Patient's consent to participate in the randomised controlled trial 7. Patient's agreement to be followed up to 12 months post-commencement of treatment

Exclusion criteria

Exclusion criteria: Does not meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
The main outcome measures were disability, health and pain. These parameters were assessed by the: 1. Aberdeen Low Back Pain Disability Scale 2. Current Perceived Health 42 (CPH42) Profile 3. Numerical Pain Scale (NRS). The NRS measures pain intensity from no pain to intolerable pain along an 11-point scale. The research assistants, who were blind to the treatment routine administered the questionnaires at baseline, then at 3, 6, and 12 weeks (short term) followed by 6, 9, 12 months (long term) after physiotherapy commenced.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

Hong Kong

Outcome results

None listed

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