Skip to content

Norwegian Psychomotor Physiotherapy in Patients With Long-lasting Musculoskeletal Pain.

Norwegian Psychomotor Physiotherapy Versus Cognitive Patient Education and Active Physiotherapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02482792
Acronym
NPMP
Enrollment
128
Registered
2015-06-26
Start date
2013-08-31
Completion date
2017-10-26
Last updated
2017-10-27

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

Conditions

Physical Disability

Keywords

Musculoskeletal disorders, Psychosomatic, Pain

Brief summary

The aim is to examine the effect of Norwegian Psychomotor Physiotherapy (NPMP) in employees with long-lasting musculoskeletal pain compared to employees receiving Cognitive Patient Education in combination with active individual physiotherapy (COPE-PT) on pain, function, quality of life and sick-leave

Detailed description

The NPMP is based on the assumption that patients with long-lasting problems, physical and/or psychological, may react with general aberrations related to posture, respiration, and movements, as well as with muscular tension and skin changes. Employees With Long lasting musculoskeletal pain problems, working in the Municipality of Bergen, will be invited to participate in an Randomized Clinical Trial (RCT), and randomized to either receive Norwegian Psychomotor Physiotherapy (NPMP) or a series of Cognitive Patient Education in combination with active individual physiotherapy (COPE-PT). The aim is to examine the effect of NPMP compared to those receiving COPE-PT on pain, function, quality of life and sick-leave.

Interventions

The recruited patients will after randomization receive either Norwegian Psychomotor Physiotherapy (NPMP) or COPE combined with active individual physiotherapy. In NPMP the treatment is individualized, targeting body-mind awareness through exercise, massage and therapeutic conversation

OTHERCognitive Patient Education and PT

The comparison group will receive a combination of education about how to manage pain (COPE) followed by active individual physiotherapy.

Sponsors

Norwegian Fund for Postgraduate Training in Physiotherapy
CollaboratorOTHER
Tove Dragesund
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 67 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients With neck,shoulder and/or widespread pain * Pain (≥ 3 Numeric Pain Rating Scale (NPRS) * Functional problems measured with Orebro Musculoskeletal Pain Screening Questionnaire (OMPSQ), Neck Disability Index (NDI) and/or Shoulder Pain and Disability Inventory (SPADI)-been sick-listed for 4-8 weeks, or on the brink of becoming sick-listed, or having had residual neck- and shoulder complaints problems during the last two years with several short-term sick-leaves. * =/6 American College of Rheumatology (ACR) tender points, * Reduced Relaxation and Flexibility from the Global Physiotherapy Examination (GPE)

Exclusion criteria

* Sick-listed \> 6 months

Design outcomes

Primary

MeasureTime frameDescription
Efficacy of Norwegian Psychomotor Physiotherapy in Patients With Long-lasting painChange from baseline in pain at 3 months, at 6 months and 12 months.Pain on the Numeric Pain Rating Scale (NPRS)

Secondary

MeasureTime frameDescription
Efficacy of Norwegian Psychomotor Physiotherapy in Patients With Long-lasting painChange from baseline in wellbeing at 3 months, at 6 months and 12 months.Wellbeing on the Short Form-12 Health Survey (SF-12)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026