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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01129817
Other study ID # 250.05.
Secondary ID
Status Completed
Phase N/A
First received May 20, 2010
Last updated May 24, 2010
Start date March 2006
Est. completion date November 2009

Study information

Verified date May 2010
Source University of Bergen
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Interventional

Clinical Trial Summary

A randomized controlled trial of the efficacy of classification based cognitive functional physiotherapy according to the system proposed by Peter O'Sullivan as compared to manual therapy and exercise in patients with non specific chronic low back pain.

The investigators hypothesis was that treatment targeted at the mechanism behind the problem from a multidimensional perspective would be superior to traditional treatment.


Description:

NSCLBP is widely viewed as a multifactorial biopsychosocial pain syndrome. It has been proposed by several authors that NSCLBP represents a vicious cycle associated with different combinations of maladaptive; cognitive (negative beliefs, fear avoidance behaviours, catastrophising, depression, stress, lack of pacing and coping), physical (pain provocative postures, movement patterns and pain behaviours) and lifestyle (inactivity, rest) behaviours that act to promote pain and disability. However a recent systematic review suggests that this change in paradigm and our new understanding of NSCLBP has not resulted in clinical trials utilizing multidimensional classification systems or targeted interventions based on the underlying mechanisms. line with this shift in paradigm a novel multidimensional classification system has been developed incorporating the biopsychosocial model, which subgroups patients based on their presentation of. with matched interventions directed at the maladaptive cognitive, physical and lifestyle behaviours associated with the disorder.


Recruitment information / eligibility

Status Completed
Enrollment 121
Est. completion date November 2009
Est. primary completion date November 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- all patients with non-specific LBP for more that 8 weeks duration

- mechanical provocation of pain with postures, movement and activities

- localised pain in the area from T12 to gluteal folds

- moderate ongoing LBP with a VAS > 2/10

- disability had to be higher than 14% on Oswestry Disability Index

Exclusion Criteria:

- sick listed for more than 4 months continuous duration

- acute exacerbation of LBP

- radicular pain with positive neural tissue provocation test

- any low limb surgery on the last 3 months

- surgery involving the lumbar spine (fusion)

- pregnancy

- psychiatric disorders - somatisation

- dominant psycho-social problems

- widespread non-specific pain disorder (no primary LBP focus)

- specific diagnoses: active rheumatologic disease, progressive neurological disease, serious cardiac or other internal medical condition, malignant basic diseases, acute traumas, infections, or acute vascular catastrophies

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Cognitive Functional Therapy
A novel multidimensional classification system has been developed incorporating the biopsychosocial model, which subgroups patients based on their presentation with matched interventions directed at the maladaptive cognitive, physical and lifestyle behaviours associated with the disorder. The intervention is called 'cognitive functional therapy' as it directly challenges these behaviours in a functionally specific and graduated manner.
Manual therapy and exercise
Patients in this group was treated with joint mobilization or manipulation techniques applied to the spine or pelvis primarily and was designed to be consistent with best current manual therapy practice in Norway. The particular dose and techniques were at the discretion of the treating therapist, based on each participant's objective and physical examination findings. In addition most of the patients in this group was given exercises or a home exercise program.

Locations

Country Name City State
Norway University of Bergen Bergen Hordaland

Sponsors (2)

Lead Sponsor Collaborator
University of Bergen Norwegian Fund for Postgraduate Training in Physiotherapy

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Pain was assessed using a pain numerical rating scale from 0 to 10 12 months No
Primary Disability Disability measured by Oswestry Disability Index. 12 months No
Secondary Well being Hopkins Symptoms Checklist. 12 months No
Secondary Beliefs Fear Avoidance Beliefs Questionnaire 12 months No
Secondary Screening questionnaire The Ørebro Pain Screening Questionnaire 12 months No
Secondary Patient satisfaction patient satisfaction. 5 items scale 12 months No
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