Nutrition Care in Patients Living With Chronic Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorLinkoeping University

About this trial

The investigators' purpose is to develop and test the feasibility, usability, and satisfaction of the Diet4painrelief app as a platform for implementing nutrition care in a specialist pain rehabilitation clinic. The Diet4painrelief will consist of two components: a) a screening tool for nutrition status b) an individually tailored behavior change program aiming to improve the dietary habits and behaviors of patients living with chronic pain.

Part I: Included 20 patients with complex chronic pain to examine the feasibility and outcomes of evidence-based Interdisciplinary Pain Rehabilitation Program (IPRP) integrated with nutrition care. The Diet4painrelief includes a screening tool to assess basic nutritional status as well as their intake of key unhealthy and healthy foods and drinks (through three 24hour-dietary recordings or food diary). Thereafter, the patients receive a personalized behavior change program for dietary optimization. The investigators will design and adapt 6 modules in the digital platform (Diet4painrelief app) based on the International Association for the Study of Pain (IASP) recommendations (6 aspects about 'nutrition and pain') and Sweden's food culture. Clinical outcomes using patient-reported data on socio-demographics, pain aspects, psychometric data, physical disability, and quality of life will be measured at three occasions: first appointment (Pre-IPRP), immediately after completing the rehabilitation program (Post-IPRP), and at a 12-month follow-up (FU-IPRP). Blood samples will be taken to identify biomarkers at the same occasions that provide objective information on metabolic and nutritional abnormalities and further to evaluate the effect of the dietary intervention on changing of pain rehabilitation outcomes.

Part II: Included 192 patients with complex chronic pain. Half of the participants receive IPRP and nutrition care (described above) and the other half receive standard IPRP.

Eligibility criteria

Qualifiers

Self reported Body Mass Index (BMI)>=25;

Written consent to participate and attend to the pain rehabilitation program due to disabling chronic pain (on sick leave or experiencing major interference in daily life due to chronic pain)

Agreement not to participate in other parallel treatments for weight reduction

Not currently using medications of weight reduction

Disqualifiers

Health conditions such as pregnancy, active metabolic disease, rheumatoid arthritis, and serious psychiatric disease (investigator's judgement, eg, psychosis or suicidal ideation);

Coagulation disorders with predisposition to bleeding, medication with anticoagulants (low- dose aspirin is permitted);

hypersensitivity to anaesthetic

Difficulties in understanding the Swedish language.

Trial design

Treatments tested in this trial

  • Nutrition care
  • Dialogue and education (part of Interdisciplinary Pain Rehabilitation Program)
  • activity training (part of Interdisciplinary Pain Rehabilitation Program)
  • meetings (part of Interdisciplinary Pain Rehabilitation Program)
  • Cognitive behavioral therapy (part of Interdisciplinary Pain Rehabilitation Program)
  • Relaxation techniques (part of Interdisciplinary Pain Rehabilitation Program)
  • Physical exercise (part of Interdisciplinary Pain Rehabilitation Program)

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Linkoeping University

Lead sponsor

Ostergotland County Council, Sweden

Collaborator