Pain in Endometriosis And the Relation to Lifestyle: Effectiveness of a Dietary Intervention and Cognitive Behavioral Therapy in Endometriosis-associated Pain

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to investigate the effect of an anti-inflammatory diet and cognitive behavioral therapy (CBT) on pain symptoms, health related quality of life and the effect on inflammatory characteristics in serum and menstruum samples as well as the effect on the gut and vaginal microbiome in women with endometriosis. In addition, we want to investigate the differences in stress (measured by hair cortisol levels), inflammatory markers in peripheral blood, menstrual effluent, and the vaginal and intestinal microbiome between persons without and with endometriosis. Participants will be randomized between standard care (control group), standard care and an anti-inflammatory diet intervention, or standard care, an anti-inflammatory diet intervention and CBT or CBT alone. Participants will follow an anti-inflammatory diet based on the Dutch Dietary Guidelines or CBT or a combination of both interventions for 12 weeks. They will receive personalized dietary advice from a dietician and recipes will be available. cognitive behavioral therapy will be administered in a total of seven individual sessions led by a psychotherapist. The content of these sessions will be psycho-education regarding pain mechanisms (and diet).

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 17
Healthy Volunteers: t
View:

• Confirmed diagnosis of endometriosis via ultrasound, MRI or surgery\*

• NRS pain score \> 4\*

• Age from 17 years

• Premenopausal status

• Body Mass Index (BMI) 18-30 kg/m2

• Ability to understand the explanation about the diet intervention (DI) and CBT\*

• Willing to follow the DI\*

• Willing to continue their use of food supplements

• Willing to undergo CBT\*

• Willing to collect menstrual effluent, and therefore willing to have two stop weeks from hormonal contraception (if applicable) during the study period.

Locations
Other Locations
Netherlands
Jeroen Bosch Hospital (JBZ)
RECRUITING
's-hertogenbosch
Rijnstate Hospital
RECRUITING
Arnhem
Amphia
RECRUITING
Breda
Catharina Hospital
RECRUITING
Eindhoven
Radboud University Medical Center
RECRUITING
Nijmegen
Contact Information
Primary
Emma Huijs
pearl-studie.verlgyn@radboudumc.nl
06-29698762
Time Frame
Start Date: 2024-10-04
Estimated Completion Date: 2027-05
Participants
Target number of participants: 250
Treatments
No_intervention: Standard care (control group)
Experimental: Standard care and an anti-inflammatory diet (DI group)
Experimental: Standard care, anti-inflammatory diet and cognitive behavioral therapy (DI + CBT group)
Experimental: Standard care and cognitive behavioral therapy (CBT group)
No_intervention: Healthy controls
Healthy controls without endometriosis
Related Therapeutic Areas
Sponsors
Collaborators: University College Cork, Université Catholique de Louvain, Horizon Europe, UNIWERSYTET MEDYCZNY W LUBLINIE, University Bonn, ZonMw: The Netherlands Organisation for Health Research and Development, SVEUCILISTE U ZAGREBU MEDICINSKI FAKULTET, University of Edinburgh, Biopsychology, Endometriosis UK, Cliniques universitaires Saint-Luc- Université Catholique de Louvain, Belgian Volition SRL, ASSOCIATION OF PEOPLE WITH ENDOMETRIOSIS I AM 1 IN 10, Wageningen University and Research
Leads: Radboud University Medical Center

This content was sourced from clinicaltrials.gov