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Somatoform Disorders clinical trials

View clinical trials related to Somatoform Disorders.

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NCT ID: NCT00625976 Completed - Clinical trials for Complex Regional Pain Syndrome Type I

Graded Exposure (GEXP) in Vivo Versus Physiotherapy in Complex Regional Pain Syndrome Type I (CRPS-I)

Start date: May 2008
Phase: N/A
Study type: Interventional

Background: Research on the treatment of CRPS-I, as described in the Dutch evidence based treatment guidelines (Richtlijn Complex Regional Pain Syndrome type I, 2006), mainly showed improvement at the level of pain and coping with pain. Only little improvement in functional restoration was found. Research in other pain populations such al neck- and back-pain patients has shown that pain related fear contributes to the development of functional disability. GEXP in vivo which aims on systematically reducing fear of movement, shows promising results in CRPS-I patients (de Jong et al., 2005). Objective: The objective of the proposed project is to compare the effectivity of GEXP in vivo with that of standardized physiotherapy in CRPS-I patients with pain related fear. Design: The study concerns a single blinded, single center, randomized clinical trial. The treatment will be preceded by two pre-measures. After treatment there will be one post-measurement and 3, 6 and 12 month follow-up measurements. Population: The study population will consist of chronic CRPS-I patients between 18 and 65, with pain related fear (PHODA-LE-score ≥ 35 and PHODA-UE-score ≥ 32). Intervention: The two interventions that will be compared are GEXP in vivo (de Jong et al., 2005) and standardized physiotherapy according to the protocol of Oerlemans, Oostendorp, de Boo en Goris (1999). The GEXP in vivo comprises 17 sessions of one hour, the physiotherapy treatment of 34 sessions of 30 minutes. Both treatments will be given over a period of 17 weeks.

NCT ID: NCT00497185 Completed - Clinical trials for Somatization Disorder

Mindfulness-based Cognitive Therapy for Patients With Functional Disorders

Start date: June 2007
Phase: N/A
Study type: Interventional

The aim of the study is to examine the efficacy of Mindfulness-Based Cognitive Therapy (MBCT) in patients with functional disorders defined as severe Bodily Distress Disorder. Hypothesis: MBCT can ameliorate the symptoms of FD defined as severe Bodily Distress Disorder and decrease health care utilization beyond the effect of shared care. Patients treated with MBCT will function better physically and socially than patients treated with shared care at 12 months' follow-up.

NCT ID: NCT00401050 Completed - Clinical trials for Patellofemoral Pain Syndrome

Comparison Study of Two Chiropractic Treatment Protocols for Knee Pain Due to Patellofemoral Pain Syndrome

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to compare outcomes of combined chiropractic care in anterior knee pain patients with patellofemoral pain syndrome.

NCT ID: NCT00368212 Completed - Clinical trials for Somatoform Disorders

Integrated Treatment Program for Hypochondriasis in Primary Care Settings

Start date: May 2005
Phase: Phase 3
Study type: Interventional

This study will evaluate the effectiveness of an integrated three-part treatment program in improving the quality of care and treatment outcomes of people with hypochondriasis in primary care settings.

NCT ID: NCT00276887 Completed - Clinical trials for Somatoform Disorders

Cognitive Behavior Therapy for Somatization Disorder

Start date: September 1999
Phase: Phase 2
Study type: Interventional

This study will examine the long-term effects of cognitive behavioral therapy on the physical symptoms, functioning, and health care utilization of people with multiple medically unexplained physical symptoms.

NCT ID: NCT00246142 Completed - Clinical trials for Myofascial Pain Syndromes

A Study of the Combination of Electrical Stimulation and Dysport® in Myofascial Pain Syndrome.

Start date: April 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether electrical stimulation enhances the effect of botulinum toxin type A (Dysport®) on myofascial pain syndrome.

NCT ID: NCT00217243 Completed - Clinical trials for Complex Regional Pain Syndromes

Evoked Fields After Median and Ulnar Stimulation

Start date: June 2005
Phase: N/A
Study type: Observational

In order to be able to study the effects of evoked fields with magnetoencephalography (MEG) in two groups of patients, comparison is made with a group of healthy volunteers.

NCT ID: NCT00166452 Completed - Clinical trials for Complex Regional Pain Syndrome, Type 1

A Study of the Effect of Lenalidamide on Complex Regional Pain Syndrome Type 1

Start date: July 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if lenalidomide is a safe and effective treatment for complex regional pain syndrome type 1 (CRPS).

NCT ID: NCT00149799 Completed - Anxiety Disorders Clinical Trials

Effectiveness of Escitalopram in the Treatment of Body Dysmorphic Disorder

Start date: May 2005
Phase: Phase 3
Study type: Interventional

This study's primary aim is to compare time to relapse and relapse rates in responders to acute escitalopram who are then randomized to placebo versus continuation treatment with escitalopram.

NCT ID: NCT00149760 Completed - Clinical trials for Somatization Disorder

Effectiveness of Cognitive-Affective Behavior Therapy for the Treatment of Somatization Disorder

Start date: August 2003
Phase: Phase 2
Study type: Interventional

This study will examine the long-term effect of cognitive-affective behavior therapy on the physical symptoms, functioning, and health care utilization of people with somatization disorder.