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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03413501
Acronym
MUD-PI
Enrollment
49
Registered
2018-01-29
Start date
2016-09-20
Completion date
2018-06-04
Last updated
2023-12-06

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

Conditions

Chronic Pain, Widespread

Brief summary

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

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).

Interventions

BEHAVIORALMUD-PI

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Patient generated indexChange in score on inclusion and 1 week after completion of intervention or control groupIndividualised patient reported outcome

Secondary

MeasureTime frameDescription
Change in EQ-5DChange in score on inclusion and 1 week after completion of intervention or control groupstandardised patient reported outcome
Change in Oswestry disability indexChange in score on inclusion and 1 week after completion of intervention or control groupstandardised patient reported outcome

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026