Efficacy of a Psychoeducative Program for Improving Quality of Life in Fibromyalgic Patients [Study Protocol]

NCT00550966 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 109

Last updated 2007-10-30

No results posted yet for this study

Summary

This research project pretends to demonstrate that a psychoeducative program implemented in the context of PC can produce a significant increase in the quality of life of patients with FM, as well as a decrease in the use of sanitary and social services, compared to usual care.

Conditions

  • Fibromyalgia

Interventions

BEHAVIORAL

Psychoeducative program in fibromyalgic patients

Multi-component program including information about the illness, counselling about physical exercise and training in autogenic relaxation. The intervention consists on nine 2 hour sessions delivered during a two month period. The pharmacological treatment prescribed by the physician is maintained in both groups.

Sponsors & Collaborators

  • Agència d'Avaluació de Tecnologia i Recerca Mèdiques

    collaborator OTHER
  • Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina

    collaborator OTHER
  • Institut Catala de Salut

    lead OTHER_GOV

Principal Investigators

  • Rita Fernández-Vergel, Doctor · Institut Català de Salut (ICS)

  • María Teresa Peñarrubia, Doctor · Institut Català de Salut (ICS)

  • Elena Blanco, Doctor · ICS

  • Mónica Jiménez, Doctor · ICS

  • Adrián Montesano, psychology · Fundació Jordi Gol i Gurina. ICS

  • Antonio Serrano, psychiatrist · Sant Joan de Déu-Serveis de Salut Mental

  • Juan Vicente Luciano, psychology · Red de Investigación en Actividades Preventivas y Promoción de la Salud en Atención Primaria (RedIAPP)

  • Mª del Camino Verduras, Doctor · ICS

  • José Miguel Ruíz, Reumatology · ICS

Study Design

Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Completion
2010-02-28

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00550966 on ClinicalTrials.gov