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The effect of various combinations of naprapathic manual therapy for patients with neck pain and/or back pain

The effect of various combinations of naprapathic manual therapy: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN92249294
Enrollment
1050
Registered
2010-02-09
Start date
2010-03-15
Completion date
Unknown
Last updated
2021-10-26

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

Conditions

Non-specific neck and/or back pain Musculoskeletal Diseases Dorsalgia

Interventions

The treatment arms being evaluated are: 1. Naprapathic manual therapy (which includes a combination of various massage techniques, stretching (both as a treatment technique and a home

Sponsors

The Scandinavian College of Naprapathic Manual Medicine (Sweden)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients 18-65 years of age who seek naprapathic therapy for a new episode of non-specific episode of neck and/or back pain with a duration of at least one week, at the student clinic at The Scandinavian College of Naprapathic Manual Medicine

Exclusion criteria

Exclusion criteria: 1. Pain level < 2 on a 10 point numerical rating scale 2. Pregnancy 3. Not fluent in the Swedish language 4. Contraindication for spinal manipulation according to SOSFS 1996:16 (The regulations and general recommendations from the Swedish National Board of Health and Welfare), such as pain caused by trauma. 5. Treatment by a naprapath, chiropractor, osteopath or a physiotherapist in the past month. 6. Specific diagnoses such as 6.1. Spondylitis 6.2. Ankylosing spondylitis (Morbus Bechterew's disease) 6.3. Disc herniation 6.4. Red flags not included in the SOSFS, above 7. Other primary pain diagnosis according to the judgment made by the therapist at the time of inclusion

Design outcomes

Primary

MeasureTime frame
1. Self rated pain and function with the use of Chronic Pain Questionnaire (CPQ) will be assessed at baseline, 7 weeks, 3, 6 and 12 months. 2. Prevalence, duration and intensity of adverse treatment reactions. This is measured with the use of a questionnaire including eight numerical rating scales (NRS 0-10) seven of which concern symptoms that has been reported in other studies after naprapathic treatment sessions or other manual therapy. The last question is ?other? in case of other symptoms experienced by the patient. Patients will answer this questionnaire when coming back to the clinic for a new treatment session.

Secondary

MeasureTime frame
1. Health related quality of life (Short-Form [SF-12]) 2. Perceived recovery (A 6-point Likert scale including ?Complete pain free and have no complaints from neck/back? to ?Is much worse?) Outcomes will be measured at baseline, 7 weeks, 3, 6 and 12 months.

Countries

Sweden

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 21, 2026