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Somatoform Disorders clinical trials

View clinical trials related to Somatoform Disorders.

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NCT ID: NCT02350296 Completed - Pain Disorders Clinical Trials

Crossover, Single Dose Randomized, Bioequivalence of Ketoprofen Lysine Salt Immediate Release vs Oral Solution

Start date: November 26, 2014
Phase: Phase 1
Study type: Interventional

Objectives: The objective of the study was to investigate the bioequivalence between two formulations containing ketoprofen lysine salt (KLS) when administered as single oral doses in two consecutive study periods to healthy male and female volunteers under fasting conditions. Primary end-point: to evaluate the bioequivalent rate (Cmax) and extent (AUC0-t) of absorption of ketoprofen after single dose administration of test and reference products. Secondary end-points: - to describe the pharmacokinetic (PK) profile of ketoprofen after single dose administration of test and reference products; - to collect safety and tolerability data after single dose administration of test and reference products.

NCT ID: NCT02346071 Completed - Clinical trials for Somatoform Disorders

Acceptance and Commitment Group Therapy for Adolescents With a Range of Functional Somatic Syndromes

Start date: January 30, 2015
Phase: N/A
Study type: Interventional

Background: An increasing number of adolescents report recurrent functional somatic symptoms. Some experience persistent symptoms and may receive functional somatic syndromes (FSS) diagnoses (i.e. symptoms not attributable to any known conventionally defined physical disease), characterised by severe disability and reduced quality of life. The aim of this study is to: 1. Develop an Acceptance and Commitment Therapy (ACT)-based group intervention for adolescents with severe FSS (conceptualized as Bodily Distress Syndrome (BDS), see detailed description). 2. Examine the efficacy of group based ACT in adolescents (aged 15-19 years) with severe FSS. The ACT-based treatment, with 9 sessions of group therapy and one follow up meeting is compared to standard treatment/enhanced usual care, which is one single advisory consultation. The study includes approximately 120 patients.

NCT ID: NCT02322515 Completed - Clinical trials for Anterior Knee Pain Syndrome

Patellar Taping on Proprioceptive Exercises in Young Women With Patellofemoral Pain Syndrome

Tapping
Start date: January 2015
Phase: N/A
Study type: Interventional

The relevance of this study is to determine the effects of a patellar taping on muscle activation of the vastus medialis oblique (VMO), vastus lateralis (VL) and gluteus medius (GM) during different proprioceptive exercises frequently utilized in rehabilitation program.

NCT ID: NCT02293083 Completed - Clinical trials for Myofascial Pain Syndrome

Hyaluronidase for Trigger Point Injection in Myofascial Pain Syndrome

Start date: April 2010
Phase: N/A
Study type: Interventional

Myofascial pain syndrome (MPS) is the most common cause of persistent regional pain characterized by myofascial trigger points. Trigger point injection (TPI) using local anesthetics is one of the most effective methods for treatment of MPS, and steroids or botulinum toxin can be added to local injections . Recent study suggested that the hyaluronan (HA) could be the basis of myofascial pain. HA within the deep fascia facilitates the free sliding of two adjacent fibrous fascial layers. If the HA assumes a more packed conformation, or more generally, if the loose connective tissue inside the fascia alters its density, the behavior of the entire deep fascia and the underlying muscle would be compromised. The investigators anticipated that hyaluronidase could decrease the viscosity of HA near the muscle and fascia of trigger points. Meanwhile, hyaluronidase is thought to promote the spread of local anesthetic solution by hydrolyzing glycosidic bonds within HA. Hyaluronidase was shown to be effective in retro- and peribulbar block for ophthalmologic surgery or reducing tissue edema in dermatology, and adhesiolysis for some interventional pain managements. However, the effect of the addition of hyaluronidase to local anesthetics during TPI has not been studied. The investigators aimed to compare the efficacy of TPI with the addition of hyaluronidase compared to local anesthetic alone on pain and quality of life in MPS patients.

NCT ID: NCT02243332 Completed - Clinical trials for Patellofemoral Pain Syndrome

Dynamic Quadriceps Muscle Stimulation for Treatment of Patellofemoral Pain

Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this small, pilot study is to evaluate a novel device that uses neuromuscular electrical stimulation to assist quadriceps muscles as a user walks. This study will involve use of this device on individuals with patellofemoral pain, a relatively common injury among active people, to see if quadriceps stimulation could mitigate disparities in quadriceps activation timing that may indirectly lead to knee pain.

NCT ID: NCT02179320 Completed - Clinical trials for Myofascial Pain Syndrome

Evaluation of the Efficacy and Neurological Effects of Dry Needling in the Treatment of Myofascial Pain Syndrome

Start date: February 2014
Phase: N/A
Study type: Interventional

AIM OF INVESTIGATION: To evaluate in a prospective, randomized, sham-controlled study the pattern of analgesic efficacy of trigger point dry needling in Myofascial Pain Syndrome (MPS) patients.

NCT ID: NCT02151500 Completed - Clinical trials for Somatoform Disorders

Stress and Health Interview for Primary Care Patients With Medically Unexplained Symptoms

Start date: May 2014
Phase: N/A
Study type: Interventional

The goal of this study is to test the feasibility and acceptability of providing an experiential assessment interview that targets emotional and stressful experiences in primary care. In this randomized, controlled trial, the investigators will compare an interview condition to a wait-list control condition. The investigators hypothesize that helping individuals first identify the links between their stress and symptoms will likely increase their awareness and endorsement of the link between stress and physical symptoms, including a willingness to engage in stress management techniques. It is also expected that helping raise an individual's awareness about their symptoms, followed by an experience and expression of unexpressed emotions is likely to influence their physical symptoms and psychological status.

NCT ID: NCT02029391 Completed - Clinical trials for Myofascial Pain Syndrome

Kinesio Taping in Subjects With Myofascial Pain Syndrome: a Randomized Controlled Trial

Start date: October 2013
Phase: N/A
Study type: Interventional

Musculoskeletal dysfunction is considered as a major public health problem affecting about one third of the adult population. Myofascial pain syndrome (MPS) characterized by myofacial trigger points as well as fascia tenderness are thought to be the main cause of musculoskeletal dysfunction. The aim of the treatment for musculoskeletal dysfunction is to reduce pain and restore normal function. Clinically, some evidence supports the application of kinesio tape in these patients. The underlying mechanism, however, is not clear. The investigators goal was to validate proposed mechanism of kinesio tape in these patients. The primary outcome are muscle stiffness, pain intensity and sensitivity.

NCT ID: NCT01989728 Completed - Depression Clinical Trials

Prevalence and Effect of Detecting Common Mental Disorders in Long-term Sickness Absence

PRW
Start date: November 2004
Phase: N/A
Study type: Interventional

The hypothesis was that a large fraction of individuals with common mental disorders were undetected in long-term sickness and that detection of the disorders by screening, a psychiatric diagnostic examination and feedback to the individuals, primary care, and rehabilitation officers improved return to work, improved quality of life and reduced psychological distress.

NCT ID: NCT01975311 Completed - Clinical trials for Patellofemoral Pain Syndrome

Effect of Lower Back Treatment in People With Patellofemoral Pain Syndrome.

Start date: October 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a lower back treatment would change the knee pain intensity and the level of functional activities as well as the muscle activities in people with anterior knee pain. The investigators hypothesized that the lower back treatment may change the hip and knee muscle activities as well as reduce the knee pain intensity and improve the functional activities in people with anterior knee pain.