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Fibromyalgia: Impact of Self-Knowledge on Well-Being

U

University of Coimbra

Status

Completed

Conditions

Fibromyalgia

Treatments

Behavioral: Self-Knowledge Training Program

Study type

Interventional

Funder types

Other

Identifiers

NCT06912971
10-2024

Details and patient eligibility

About

The goal of this observational study is to evaluate the impact of self-knowledge training on the well-being of individuals with fibromyalgia. The main questions it aims to answer are:

Does self-knowledge training improve participants' perceived quality of life?

Does self-knowledge training influence the way participants manage their fibromyalgia symptoms?

Participants will:

Take part in a structured self-knowledge intervention based on the Enneagram framework.

Complete validated questionnaires before and after the intervention to assess their well-being.

Provide qualitative feedback on their experience with the training.

This study will help understand whether self-awareness strategies can be integrated into non-pharmacological approaches for fibromyalgia management.

Enrollment

16 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of fibromyalgia
  • Age ≥ 18 years
  • Ability to understand and provide informed consent

Exclusion criteria

  • Cognitive impairment that prevents comprehension of the intervention

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

16 participants in 2 patient groups

Self-Knowledge Training Group
Experimental group
Description:
Participants in this group will undergo a self-knowledge training program based on the Enneagram framework. The program consists of 2 sessions, focusing on self-awareness, emotional regulation, and personal growth.
Treatment:
Behavioral: Self-Knowledge Training Program
Control Group
No Intervention group
Description:
Participants in this group will not receive any self-knowledge training during the study period. They will continue with their usual care and will be assessed at the same time points as the intervention group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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