EndometriosisEndometriosis Related PainEndometriosis, PainEndometriosis-related PainPainPain Intensity AssessmentPain ManagementPain, Chronic DiseasePain ScoreTherapeutic ExerciseExercise AdherenceAdherence, TreatmentTreatment Adherence and ComplianceQuality of Life
Investigational drug(s) / intervention(s)
PAIN NEUROSCIENCE EDUCATION AND THERAPEUTIC EXERCISE PROGRAMUSUAL CARE
PAIN NEUROSCIENCE EDUCATION AND THERAPEUTIC EXERCISE PROGRAM: PAIN NEUROSCIENCE EDUCATION
1\. Introduction to the knowledge of pain in the XXI century. Pain as an alarm system.
Types of pain. Differences between acute and chronic pain. 3. Chronic pain. Concepts of kinesiophobia, catastrophism and fear avoidance, self-determination and neuroplasticity.
4\. Main pain management tools based on scientific evidence. 5. . Transtheoretical model of change. Adherence to treatment, importance as a determinant in health.
6\. Messages for home. Strategies of active coping in the maintenance stage.
THERAPEUTIC EXERCISE PROGRAM 10-min warm-up. Joint mobility exercises with dual task or gamification. 30-min main part. Sequence of balance work between strength and body flexibility dosed according to the specific needs of each participant.
10-min cool down including breathing exercises and motor imagery. Home exercise program: walking (150 minutes in total, 3 days alternating with the face-to-face sessions).
USUAL CARE: The treatment provided is mainly pharmacological, adjusted to the symptomatic profile of theses patients.
Conventional medical care is based on hormonal, pharmacological and/or surgical treatment and is carried out on an individualized basis depending on the severity of the disease and the patient's needs, especially in matters of desire to become pregnant. Surgical treatment is carried out when pharmacological therapy (hormonal or anti-inflammatory) is ineffective or involves adverse events.
Study summary
The main objective of this study is to know if the application of both therapies, neuroscience pain education plus therapeutic exercise will modify pain, catastrophizing and quality of life in endometriosis.
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Adult women (over 18 years of age) diagnosed with endometriosis.
* Women with the capacity to carry out a therapeutic program based on muscular exercise.
* Women with the capacity to understand the requirements of the study.
Exclusion Criteria:
* Women undergoing fertility and/or assisted reproduction treatment.
* Pregnant women.
Primary outcome measure(s)
Change from Self-report Pain magnitude — At the start of the study (at baseline, 0 week), 1 month and 2 months after the start of the intervention (4 and 8 weeks), 1 month from the last session (12th week), 3 months from the last session (20th week) and 6 months from the last session (32th week Magnitude of chronic pain: Chronic pain grading scale. Likert-type scale with 8 items that are evaluated between 0 and 10 for items 2, 3, 4, 6, 7 and 8. Item 1 collects the number of days with pain in the last six months. Item 5 rates the impediment to the performance of usual tasks in the last three months, and can be evaluated between none and 90. The higher the score, the greater the chronic pain involvement. If the score is zero, the patient will be rated as having no pain. Chronic pain will be of low interference with grade I (low intensity) or grade II (high intensity) or of high interference with grade III (moderately limiting) or grade IV (severely limiting). Persistence will be graded as non-persistent or persistent pain.
Treatment Compliance — From enrollment to the end of treatment at 8 weeks Self-report of the person responsible for managing attendance at the group sessions in the experimental group. Participants who attend 80% or more of the sessions will be considered compliant.
Treatment adherence (Maintenance of the therapeutic exercise program at home ) — From the end of the intervention at 8 weeks (starting at week 9) to the end of treatment at 32 weeks. Adherence to treatment (experimental group), measured by visual analogue scale (VAS) included in the patient diary, in terms of:
Maintenance of treatment at home: number of days that the proposed exercise is performed (100% being 2 times a week). Each patient will complete the VAS scale monthly. Participants with a score equal to or greater than 8 points out of 10 on the VAS scale will be considered to have high adherence.
Changes from Self-report pain catastrophizing — At the start of the study (at baseline, 0 week), 1 month and 2 months after the start of the intervention (4 and 8 weeks), 1 month from the last session (12th week), 3 months from the last session (20th week) and 6 months from the last session (32th week Catastrophizing thoughts in the face of pain: Pain Catastrophizing Scale (PCS). Pain catastrophizing is a construct that is related to a negative and exaggerated orientation towards painful stimuli. The scale, validated in Spanish, is a list of 13 statements that describe different thoughts and feelings that may be related to pain in the dimensions of rumination, magnification and hopelessness. The person indicates the degree to which he/she has such thoughts or feelings by rating them between 0 (not at all) and 4 (all the time). The theoretical range of the instrument is between 13 and 62, with higher values indicating a higher index of catastrophizing.
Change from Self-report specific quality of life — At the start of the study (at baseline, 0 week), 1 month and 2 months after the start of the intervention (4 and 8 weeks), 1 month from the last session (12th week), 3 months from the last session (20th week) and 6 months from the last session (32th week Specific quality of life: Endometriosis Health Profile (EHP-30+23) questionnaire Spanish version. The questionnaire is composed of two parts. Part 1 with 30 itmens and part 2 divided into five subscales: pain, control and helplessness, emotional well-being, social support and self-image. For part 1 and each subscale a total score is created as a percentage of the maximum possible score. 0 is considered the best possible health status and 100 the worst.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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