Norwegian Psychomotor Physiotherapy - The Effect on Quality of Life

NCT ID: NCT02282007

Last Updated: 2022-10-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 105 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-02-28
• Study Completion Date: 2018-07-31

Brief Summary

More and more people suffer from stress-related illness and ailments that can greatly affect the individual's experienced quality of life and sense of coping since pain, physical, mental and social functioning are closely linked. Many of these people will seek primary care for help, and thus be referred to the Norwegian psychomotor physiotherapy (NPMP) performed by physiotherapists in primary care.

Data shows that for the first three months of 2009, 42% of patients were referred to NPMP had a musculoskeletal diagnosis as the first diagnosis, often in the form of long-term and comprehensive pain problems. Many of the patients also had emotional difficulties, but without being diagnosed with mental illness. 23% of patients who were referred to NPMP had a psychiatric diagnosis as the first diagnosis. The full range of psychiatric diagnoses are represented, but the majority of patients were treated for anxiety and depression.

The investigators want to let people who have had NPMP treatment to consider what effect the treatment has given, measured by separate registrations of quality of life, pain, physical, mental and social functioning.

Detailed Description

The primary aim of this is project intends to evaluate the effect of Norwegian psychomotor physiotherapy (NPMP) on Health related Quality of Life measured by Short-form Health Survey (SF-36). The secondary aims are to evaluate the effect of Norwegian psychomotor physiotherapy (NPMP) on the variables Subjective Health Complaints Inventory (SHC); Hopkins 's Symptom Check List , Örebro Screening for musculo-skeletal pain ,Numeric Pain Rating Scale , Oslo Social Support Scale , Coping and The self-esteem scale"

The study design is based on the guidelines for randomized controlled trials presented in the CONSORT statement. The study will address to people who have had NPMP treatment approach, and they will be asked to consider what effect the treatment has given, measured by separate registrations of quality of life, pain, physical, mental and social functioning.

Participants Power calculation based on the primary outcome Short-form Health Survey (SF-36) proved that minimum 170 participants must be recruited. The participants will be recruited among patients on the waiting list for NPMP by all psychomotor physiotherapists who are members of the Norwegian Physiotherapists Association. If patients want to participate in the study, they will be randomized to an intervention group and a control group by drawing lots.

The intervention group will have NPMP as usual in 6 months. The control group remains on the waiting list for 6 months. Participants in both groups will be asked to fill out the self-assessment questionnaire at the start of the project and at the completion of the project after six months. Participants in the intervention group will receive the same form after 12 months, to examine whether there have been any subsequent change after completion NPMF.

Timing of surveys:

Participants will be given questionnaires by the NPMP physiotherapist at

• Baseline - 2 weeks before NPMF (both groups)
• After 6 months (both groups)
• After 12 months (intervention group).

Conditions

Pain; Stress; Psychosomatic Diseases; Muscle Skeletal Disorders

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

No Intervention:Control group

Group Type: NO_INTERVENTION

No interventions assigned to this group

Individual NPMP to the participants

This arm will receive NPMP for 6 months, individually adjusted to their problems.

Group Type: EXPERIMENTAL

Individual NPMP to the participants

Intervention Type: BEHAVIORAL

The participants in the intervention group will receive NPMP individually adjusted for six months. NPMP is not a standardized treatment approach, but individually adjusted to the individual patient according to their individual problems.

Interventions

Individual NPMP to the participants

The participants in the intervention group will receive NPMP individually adjusted for six months. NPMP is not a standardized treatment approach, but individually adjusted to the individual patient according to their individual problems.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

1. Being referred to NPMP

2. Being able to give informed consent

3. The therapist finds the NPMP to be a proper treatment to this patient

Exclusion Criteria

1. Do not understand Norwegian

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Oslo Metropolitan University

OTHER

Sponsor Role: lead

Responsible Party

Astrid Bergland

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Astrid Bergland, Phd

Role: PRINCIPAL_INVESTIGATOR

Oslo Metropolitan University

Locations

Oslo and Akershus University College of Applied Sciences

Oslo, , Norway

HIOA

Oslo, , Norway

Countries

Norway

Other Identifiers

REK 2013/1913

Identifier Type: -

Identifier Source: org_study_id