- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07661745
Interdisciplinary Program to Improve Quality of Life in People With Fibromyalgia
Evaluation of an Optimized Interdisciplinary Program to Improve Quality of Life in People With Fibromyalgia: A Quasi-Experimental Study
Fibromyalgia is a chronic condition characterized by widespread pain, fatigue, sleep disturbances, and psychological symptoms that significantly affect quality of life. This quasi-experimental study aims to evaluate the effectiveness of the FIBROCatCentral interdisciplinary program in improving health-related quality of life among adults with fibromyalgia receiving care in Primary Care centers in Central Catalonia, Spain.
Participants in the intervention group will attend a structured multidisciplinary program consisting of 24 sessions delivered by healthcare professionals from different disciplines, including nursing, medicine, physiotherapy, nutrition, mental health, social work, and pharmacy. Outcomes will be assessed at baseline and at 3, 6, and 12 months. The primary outcome is health-related quality of life measured using the EuroQol-5D questionnaire. Secondary outcomes include fibromyalgia impact, depressive symptoms, treatment adherence, participant satisfaction, and changes in pharmacological treatment.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Fibromyalgia is a chronic syndrome characterized by widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive symptoms, and psychological distress. The condition has a substantial impact on quality of life and represents a significant burden for healthcare systems due to frequent healthcare utilization and long-term management needs.
Current evidence suggests that isolated pharmacological approaches provide limited benefits. Consequently, multidisciplinary and multicomponent non-pharmacological interventions incorporating physical activity, health education, psychological support, and self-management strategies have emerged as promising approaches for improving patient outcomes.
The FIBROCatCentral study is a quasi-experimental pre-post intervention study designed to evaluate the effectiveness of an optimized interdisciplinary program for people with fibromyalgia in Primary Care settings in Central Catalonia. The study will be conducted in Primary Care centers belonging to the Catalonia Central Health Region of the Catalan Health Institute (ICS).
Eligible participants will be adults aged 18 to 85 years with a diagnosis of fibromyalgia assigned to participating Primary Care centers. Participants choosing to participate in the intervention will be allocated to the intervention group, while those who decline participation in the program but agree to study participation will form the control group and continue receiving usual care.
The intervention consists of 24 one-hour sessions delivered by an interdisciplinary team including nurses, physicians, physiotherapists, emotional well-being professionals, nutritionists, social workers, and pharmacists. The program combines educational and practical activities aimed at improving symptom self-management, physical functioning, emotional well-being, and overall quality of life.
Data will be collected at baseline and at 3, 6, and 12 months using validated questionnaires. The primary outcome will be health-related quality of life assessed with the EuroQol-5D (EQ-5D). Secondary outcomes will include fibromyalgia impact measured with the Revised Fibromyalgia Impact Questionnaire (FIQ-R), depressive symptoms measured with the Patient Health Questionnaire-9 (PHQ-9), treatment adherence, participant satisfaction, and changes in pharmacological treatment.
The study hypothesis is that participation in the FIBROCatCentral interdisciplinary program will significantly improve quality of life and fibromyalgia-related symptoms compared with usual care.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Barcelona
-
Manresa, Barcelona, Spanien, 08240
- Institut Català de la Salut - Gerència Territorial Catalunya Central
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Diagnosis of fibromyalgia.
- Age between 18 and 85 years.
- Assigned to a participating Primary Care Center in the Central Catalonia region (Bages, Berguedà, Moianès, or Calaf areas).
- Ability and willingness to provide written informed consent.
Exclusion Criteria:
- Severe mental illness.
- Current follow-up in a specialized hospital fibromyalgia unit and previous participation in a therapeutic group program for fibromyalgia.
- Inability to complete study questionnaires due to language barriers, illiteracy, or other limitations affecting reading or writing.
- Refusal or inability to provide informed consent.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Intervention
Participants will receive the FIBROCatCentral interdisciplinary program consisting of 24 one-hour sessions delivered by an interdisciplinary team including nurses, physicians, physiotherapists, emotional well-being professionals, nutritionists, social workers, and pharmacists.
The program combines educational and practical activities aimed at improving symptom self-management, quality of life, and overall well-being.
|
A 24-session interdisciplinary program for people with fibromyalgia delivered by primary care healthcare professionals, including nurses, physicians, physiotherapists, emotional well-being professionals, nutritionists, social workers, and pharmacists.
The intervention combines educational and practical activities aimed at improving symptom self-management, quality of life, and overall well-being.
|
|
Kein Eingriff: Control
Participants will continue receiving usual care in Primary Care, including routine follow-up visits and pharmacological management of symptoms as determined by their healthcare professionals.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Fibromyalgia Impact
Zeitfenster: Baseline, 3 months, 6 months, and 12 months
|
Fibromyalgia impact assessed using the Revised Fibromyalgia Impact Questionnaire (FIQ-R).
|
Baseline, 3 months, 6 months, and 12 months
|
|
Health-Related Quality of Life
Zeitfenster: Baseline, 3 months, 6 months, and 12 months
|
Health-related quality of life assessed using the EuroQol-5D (EQ-5D) questionnaire.
|
Baseline, 3 months, 6 months, and 12 months
|
|
Depressive Symptoms
Zeitfenster: Baseline, 3 months, 6 months, and 12 months
|
Depressive symptoms assessed using the Patient Health Questionnaire-9 (PHQ-9).
|
Baseline, 3 months, 6 months, and 12 months
|
Mitarbeiter und Ermittler
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- Wolfe F, Clauw DJ, Fitzcharles MA, Goldenberg DL, Hauser W, Katz RL, Mease PJ, Russell AS, Russell IJ, Walitt B. 2016 Revisions to the 2010/2011 fibromyalgia diagnostic criteria. Semin Arthritis Rheum. 2016 Dec;46(3):319-329. doi: 10.1016/j.semarthrit.2016.08.012. Epub 2016 Aug 30.
- Sauch Valmana G, Miro Catalina Q, Carrasco-Querol N, Vidal-Alaball J. Gender, Mental Health and Socioeconomic Differences in Fibromyalgia: A Retrospective Cohort Study Using Real-World Data from Catalonia. Healthcare (Basel). 2023 Feb 10;11(4):530. doi: 10.3390/healthcare11040530.
- Serrat M, Almirall M, Muste M, Sanabria-Mazo JP, Feliu-Soler A, Mendez-Ulrich JL, Luciano JV, Sanz A. Effectiveness of a Multicomponent Treatment for Fibromyalgia Based on Pain Neuroscience Education, Exercise Therapy, Psychological Support, and Nature Exposure (NAT-FM): A Pragmatic Randomized Controlled Trial. J Clin Med. 2020 Oct 18;9(10):3348. doi: 10.3390/jcm9103348.
- Ollevier A, Vanneuville I, Carron P, Baetens T, Goderis T, Gabriel L, Van de Velde D. A 12-week multicomponent therapy in fibromyalgia improves health but not in concomitant moderate depression, an exploratory pilot study. Disabil Rehabil. 2020 Jun;42(13):1886-1893. doi: 10.1080/09638288.2018.1543361. Epub 2019 Jan 29.
- Luciano JV, Martinez N, Penarrubia-Maria MT, Fernandez-Vergel R, Garcia-Campayo J, Verduras C, Blanco ME, Jimenez M, Ruiz JM, Lopez del Hoyo Y, Serrano-Blanco A; FibroQoL Study Group. Effectiveness of a psychoeducational treatment program implemented in general practice for fibromyalgia patients: a randomized controlled trial. Clin J Pain. 2011 Jun;27(5):383-91. doi: 10.1097/AJP.0b013e31820b131c.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Schmerzen
- Neurologische Manifestationen
- Erkrankungen des Bewegungsapparates
- Erkrankungen des Nervensystems
- Muskelerkrankungen
- Neuromuskuläre Erkrankungen
- Rheumatische Erkrankungen
- Verhaltenssymptome
- Pathologische Zustände, Anzeichen und Symptome
- Verhalten
- Anzeichen und Symptome
- Fibromyalgie
- Chronischer Schmerz
- Depression
Andere Studien-ID-Nummern
- FibroCatCentral-23/199-P
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Fibromyalgie (FM)
-
Fundació Institut de Recerca de l'Hospital de la...AbgeschlossenFibromyalgie (FM)Spanien
-
University of UtahRekrutierungFibromyalgie (FM)Vereinigte Staaten
-
Ionclinics & Deionic SLHospital Clínico Universitario de ValenciaNoch keine RekrutierungFibromyalgie (FM)Spanien
-
Ain Shams UniversityRekrutierung
-
Hospital de Clinicas de Porto AlegreRekrutierungtDCS | EEG | Duloxetin | Fibromyalgie (FM) | BDNFBrasilien
-
Sultan Abdulhamid Han Training and Research Hospital...Noch keine RekrutierungZentrale Sensibilisierung | Schmerzwahrnehmung | Quantitative sensorische Prüfung | Fibromyalgie (FM) | DRUCKSCHMERZSCHWELLE
-
Ankara Training and Research HospitalAbgeschlossenFibromyalgie (FM) | Myokardfunktion | Subklinische ventrikuläre DysfunktionTürkei (türkiye)
-
Universitair Ziekenhuis BrusselRekrutierungReizdarmsyndrom (IBS) | Fibromyalgie (FM)Belgien
-
European University Miguel de CervantesRekrutierungFibromyalgie (FM)Spanien
-
Universidad Nacional Andres BelloNoch keine Rekrutierung
Klinische Studien zur FIBROCatCentral Multidisciplinary Intervention Program
-
Mansoura UniversityUniversity of PittsburghAbgeschlossenSchizophrenie | Stigma, sozialÄgypten
-
University of BernAktiv, nicht rekrutierendDurchführbarkeit | Suizidgedanken | Selbstmord, versucht | Kosteneffektivität | ProzessfaktorenSchweiz
-
Syracuse UniversityTexas Woman's UniversityAbgeschlossenAutismus-Spektrum-StörungenVereinigte Staaten
-
Medical University of South CarolinaKaiser PermanenteRekrutierungGewalt, körperlich | SchusswaffenverletzungVereinigte Staaten
-
University of Texas at AustinNational Institute on Disability, Independent Living, and Rehabilitation ResearchAbgeschlossenAutismus-Spektrum-StörungVereinigte Staaten
-
IWK Health CentreCanadian Institutes of Health Research (CIHR)AbgeschlossenOppositionelles Trotzverhalten | VerhaltensstörungKanada
-
University of ChicagoNational Heart, Lung, and Blood Institute (NHLBI); COPD Foundation; Society of... und andere MitarbeiterRekrutierungCOPD | COPD Exazerbation AkutVereinigte Staaten
-
University Hospital, BrestRekrutierung
-
Ajou University School of MedicineKorea Health Industry Development Institute; Sungshin Women's UniversityRekrutierungJugendsuizid und Selbstverletzung Intervention: Klinische und biologische Ergebnisse Studie (SHIELD)Suizidgedanken | Selbstmord, versucht | Selbstverletzendes VerhaltenSüdkorea
-
Consorcio Centro de Investigación Biomédica en...Hospital Clinic of Barcelona; Hospital Universitario La Paz; Hospital General... und andere MitarbeiterAbgeschlossenChronischer Schmerz | Schlafen | Zirkadiane RhythmusstörungenSpanien