A Multi-disciplinary Pain Intervention (MUD-PI) for Patients With Chronic Widespread Primary Pain

NCT ID: NCT03413501

Last Updated: 2023-12-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

49 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-09-20

Study Completion Date

2018-06-04

Brief Summary

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Patients who fulfilled inclusion criteria and consented to participate received either treatment as usual at the clinic, or were enrolled in a group-therapy based intervention, the multi-disciplinary pain intervention, led by a Medical doctor, physiotherapist and psychologist at the clinic.

Detailed Description

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The Department of Pain Management and Research at Oslo University Hospital is Norway's largest outpatient pain clinic. It treats around one thousand new patients annually suffering from chronic pain of all aetiologies. Many of the patients receive interdisciplinary care based on a biopsychosocial framework, by at least two health care providers (physician, physiotherapist, psychologist, occupational therapist and/or nurse).

Participants were recruited through referrals from primary or secondary care, which were identified by an established interdisciplinary team. Patients found potentially eligible for the study were contacted by the research team and consulted with a research physician. Patients who fulfilled the inclusion criteria were invited to participate in the study and signed a consent form. Patients who declined to participate and non-eligible patients received usual care.

Inclusion criteria were 1) age 18 or more; 2) pain in at least three out of five bodily regions (defined as the four quadrants and axially); 3) pain persisting three months or more; 4) the patient was able to give informed consent and benefit from group therapy (including sufficient cognitive capacity and language skills); 5) no other medical condition could better explain the symptoms.

Subjects were randomised either to treatment as usual or a group-based multidisciplinary pain intervention (the MUD-PI).

Conditions

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Chronic Pain, Widespread

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Treatment as usual

Receives treatment as usual at the clinic

Group Type NO_INTERVENTION

No interventions assigned to this group

MUD-PI

Receives multi-disciplinary pain intervention, agroup-based, multi-disciplinary treatment

Group Type EXPERIMENTAL

MUD-PI

Intervention Type BEHAVIORAL

Interventions

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MUD-PI

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age 18 or more
* Pain in at least three out of five bodily regions (defined as the four quadrants and axially)
* Pain persisting three months or more
* The patient was able to give informed consent and benefit from group therapy (including sufficient cognitive capacity and language skills
* No other medical condition could better explain the symptoms.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Oslo University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Lars-Petter Granan

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

References

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Tschudi-Madsen H, Rodevand LN, Boymo Kaarbo M, Granan LP. Chronic Widespread Pain in a tertiary pain clinic: classification overlap and use of a patient generated quality of life instrument. Scand J Pain. 2019 Apr 24;19(2):245-255. doi: 10.1515/sjpain-2018-0097.

Reference Type DERIVED
PMID: 30465720 (View on PubMed)

Other Identifiers

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OsloUH Smerteklinikken

Identifier Type: -

Identifier Source: org_study_id