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Sense of Coherence and Empowerment at Patients With MUPS

Not Applicable
Recruiting
Conditions
Medically Unexplained Symptoms
Sense of Coherence
Interventions
Behavioral: Metacognitive Therapy
Registration Number
NCT05121922
Lead Sponsor
University of Oslo
Brief Summary

This is a study on Metacognitive therapy in general practice in Norway. The intervention is a small pilot study to examine whether Metacognitive therapy is feasible in an ordinary general practice. Will the physicians be capable to learn and provide the therapy method for their patients with MUPS and is is possible to implement this in an ordinary general practice routine? Both physicians and their patients will be asked to respond to a questionnaire on perceived utility of the treatment.

Detailed Description

Metacognitive therapy is different from Cognitive therapy in the sense that it adresses the individual's attention towards potential worries and threats and also the management performed by the patient to avoid these. Also the individual's capacity to produce empowerment to manage these threats are of interest in the talks with the health care provider. - In this study, General Practitioners with specific training in Metacognitive therapy will be asked to recruit 2-3 patients with Medically Unexplained Physical Symptoms each and invite them to a series of Metacognitive Therapy. The patients and physicians will then provide their assessments of the treatment on a number of questionnaires. To explore the Sense of coherence and Empowerment among patients with Medically Unexplained Symptoms, the physicians will be asked to recruit six patients each to respond to a questionnaire.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • MUPS: Medically Unexplained Physical Symptoms
  • somatic and mental examination sufficiently accomplished
  • ongoing symptoms
  • more than three months of disabeling symptoms
Exclusion Criteria
  • not capable to respond on a written questionnaire in Norwegian

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
InterventionMetacognitive TherapyAll patients recieve active treatment
Primary Outcome Measures
NameTimeMethod
Feasibility in daily practiceOne year

The physicians will record the number of patients that agree to participate and complete the treatment

Secondary Outcome Measures
NameTimeMethod
Effect of metacognitive therapyOne year

Participating patients will respond on The Short Form Health Survey RAND-36 at start and at the end of the treatment. A reduced score indicates improvement of symptom burden.

Trial Locations

Locations (1)

University of Oslo

🇳🇴

Oslo, Norway

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