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Somatoform Disorders clinical trials

View clinical trials related to Somatoform Disorders.

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NCT ID: NCT03762213 Completed - Clinical trials for Complex Regional Pain Syndromes

Audio-Visual Relaxation Technology for Pediatric Amplified Musculoskeletal Pain Syndrome

Start date: December 20, 2018
Phase: N/A
Study type: Interventional

A pilot randomized controlled trial to assess feasibility, acceptability and generate outcome domains for a future RCT testing the efficacy of immersive virtual reality on pain intensity in pediatric amplified musculoskeletal pain syndrome.

NCT ID: NCT03755817 Completed - Pain Syndrome Clinical Trials

Efficacy Assessment of SCENAR Device on Common Spinal Pain Syndrome

SCENAR1
Start date: November 14, 2018
Phase: N/A
Study type: Interventional

Randomized, singled blinded, controlled trial of the efficacy of a SCENAR session in patients with vertebral pain. SCENAR is an electrotherapy device.

NCT ID: NCT03755375 Completed - Clinical trials for Interstitial Cystitis

Physiotherapeutic Interventions Applied to the Bladder Pain Syndrome

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

Related to urological and gynecological systems, patients with Bladdeer Pain Syndrome (BPS) often present pain, pressure and chronic discomfort in suprapubic and perineal area associated with low urinary tract symptoms. This condition can generates a negative impact in cognitive, social, behavioral and sexual quality of life. As Bladder Pain Syndrome originates from different causes and includes the genitourinary, gastrointestinal, musculoskeletal and neuropsychological systems, a multidisciplinary approach is needed with doctors,physiotherapists, psychologists and others. Physiotherapeutic interventions are recommended as a conservative treatment for patients with BPS. The physiotherapeutic interventions include the use of Biofeedback to relax the pelvic floor muscles and manual therapy (myofascial trigger points release) to decrease muscle tension. Transcutaneous electrostimulation (TENS) is used to decrease the pain and postural exercises to improve the pelvic mobility. In this study, our hypothesis was that women with BPS presented musculoskeletal dysfunction, and we tested a different physiotherapy approach that was not being used. The reason for that understanding was the presence of refractory urinary and pain symptoms notwithstanding the physiotherapy conventional treatment, such as manual therapy and biofeedback. To test our hypothesis, we decided to add either TENS or postural exercises to the conventional treatment. The objective of this study was to verify the effects of biofeedback (BF) and manual therapy (MT) associated with transcutaneous electrical nerve stimulation (TENS) or postural exercises (PE) in the treatment of bladder pain syndrome (BPS) in women regarding pain and urinary symptoms.

NCT ID: NCT03720587 Completed - Clinical trials for Greater Trochanteric Pain Syndrome

The Experiences of Patients With Greater Trochanteric Pain Syndrome.

Start date: December 1, 2018
Phase:
Study type: Observational

Greater Trochanteric Pain syndrome (GTPS) is a debilitating condition causing pain on the outside of the hip. This study aims to explore the experiences, beliefs and expectations of patients with GTPS, using semi-structured interviews.

NCT ID: NCT03717532 Terminated - Clinical trials for Patellofemoral Pain Syndrome

Blood Flow Restriction Therapy in Patellofemoral Pain Syndrome

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of blood restriction therapy by comparing increase in muscle mass and strength in patients that receive blood restriction therapy to patients who receive a placebo.

NCT ID: NCT03709797 Recruiting - Clinical trials for Spinal Cord Injuries

Effectiveness of Dry Needling as a Treatment of Shoulder Myofascial Pain Syndrome in Spinal Cord Injury Patients

Start date: November 9, 2018
Phase: N/A
Study type: Interventional

Shoulder pain in people with spinal cord injury is one of the most prevalent in acute and chronic patients because of weakness in shoulder periarticular muscles, and also because of overuse of these part of the body in assistive devices. This study aims to evidence if dry needling (a physiotherapy technique) is also useful in patients with spinal cord injury, and how long it could hold out without or less pain.

NCT ID: NCT03686748 Recruiting - Low Back Pain Clinical Trials

Two Point Discrimination

TPD
Start date: July 21, 2018
Phase: Early Phase 1
Study type: Interventional

SPECIFIC AIMS Pain in both youth and adults is a complex, subjective and personal experience, and remains poorly understood. One particularly perplexing dimension of some forms of pain is the tendency of pain to spread outside of an affected body site to adjacent location, and then to unaffected body sites. Such widespread pain may reflect an altered spatial tuning of somatosensory processing, such that lateral inhibition is diminished, thereby allowing pain to spread. To date, no therapies exist which are designed specifically to diminish or even reverse the spatial spread of pain. However, training in two-point discrimination holds the potential to retune spatial aspects of somatosensory processing and may represent a novel therapy for widespread pain. Thus, the present investigation will test the following aims: Aim 1. Do youth with chronic pain have disrupted spatial tuning of somatosensory processing? Deficits in two point tactile discrimination have long been noted in adults with chronic pain, but such deficits remain poorly documented in pediatric chronic pain patients. In order to determine if such deficits exist, youth with both chronic pain and healthy youth will undergo assessment of two point discrimination thresholds. Aim 2. Does two-point discrimination training result in diminished pain and disability in youth with somatic pain? After initial characterization of tactile discrimination thresholds, youth with chronic pain will participate in multiple sessions of either two-point discrimination training or a single-point spatially-directed attentional control condition. Training will involve up to 9 additional sessions. Efficacy of training will be assessed by 1) reductions in the spatial extent of pain, 2) reductions in pain intensity and unpleasantness, and 3) reductions in pain-related disability.

NCT ID: NCT03685812 Completed - Clinical trials for Patellofemoral Pain Syndrome

Validity and Reliability of Autocad Software Assessment of JPS in PFPS

Start date: September 25, 2018
Phase:
Study type: Observational

The overall aim of the study is to assess the reliability and validity of Autocad software to measure JPS in PFPS, especially: 1. To assess the intra-tester and between day reliability of measurement of JPS using Autocad software. 2. To assess the validity of these measurements against those found during an IKD.

NCT ID: NCT03682601 Terminated - Dyspareunia Clinical Trials

Sexual Penetration Pain in Postmenopausal Women: A Topical Botanical Drug Treatment

Start date: August 30, 2018
Phase: Phase 2
Study type: Interventional

This study will evaluate the use of topical 5 or 10% sinecatechins, a botanical drug derived from green tea for the alleviation of sexual pain in the area around the vaginal opening (the vulvar vestibule), that is a main source of pain during sexual contact or dyspareunia, in postmenopausal women, with vulvovaginal atrophy. Women may or may not be using estrogens. Half of the women will receive the study drug, 5 or 10% sinecatechins and half will receive placebo. In addition to the reduction or elimination of pain upon penetration, women may also experience increase in lubrication, arousal and intensity of orgasm

NCT ID: NCT03671993 Completed - Clinical trials for Pelvic Pain Syndrome

Clinical Effect Observation for Electrical Pudendal Nerve Stimulation in Treating Urethral Pain Syndrome

Start date: October 5, 2018
Phase: N/A
Study type: Interventional

In this randomized controlled trial, we intend to determine whether electrical pudendal nerve stimulation is more effective than intravesical instillation in urethral pain syndrome.