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Treatment clinical trials

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NCT ID: NCT03856333 Completed - Treatment Clinical Trials

Cognitive Exercise Therapy Approach Scale in Patients With Chronic Neck Pain

Start date: January 31, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to determine the validity, reliability and sensitivity of the Cognitive Exercise Therapy Approach Scale in patients with neck pain.

NCT ID: NCT03746808 Completed - Clinical trials for Alcohol Use Disorder

Development and Testing of a Just-in-Time Adaptive Smart Phone Intervention to Reduce Drinking Among Homeless Adults

Smart-T
Start date: February 14, 2019
Phase: N/A
Study type: Interventional

Homeless adults are 8 times as likely to be alcohol dependent compared with adults in the general population, yet few studies have examined the precipitants of alcohol use in this vulnerable population. Ecological momentary assessments (EMAs) that involve repeated assessment of thoughts/mood/behaviors (e.g., via smart phone) is currently the most accurate way to assess individuals in real-time in their natural environments. Advances in smartphone technology also allow for the collection of continuous geolocation and other passive sensing data. Thus, researchers can now link environmental risks and protective factors to outcomes, without reliance on subjective reporting alone. Building on prior work, this study will use a three-phase study to develop and test a "just in time" adaptive intervention to reduce alcohol use in homeless men and women. Phase I will use smartphones and passive sensing technologies to monitor geolocation, psychosocial variables (e.g., stress, affect, urge to drink), and alcohol use in a group of 80 homeless adults with an AUD who are receiving shelter-based treatment. Phase I will identify environmental (i.e., geolocation), cognitive, and behavioral antecedents of alcohol use over 4 weeks. Phase II will use this information to create a risk algorithm and tailored treatment messages that anticipate and intervene to prevent drinking. The resulting app will assess imminent risk of alcohol use after each EMA and will deliver relevant treatment messages that match a person's current risk factors. Phase III will test the feasibility, acceptability and preliminary efficacy of the app in a sample of 40 homeless adults with an AUD who receive the EMA plus treatment messages over 4 weeks. Drinking will be determined via self-report, supplemented by a transdermal alcohol sensor (i.e., SCRAM) worn by participants. This project will be the first to combine geolocation and psychosocial variables to identify real-time antecedents of drinking. If effective, this smartphone app could significantly improve treatment engagement, drinking outcomes, and quality of life among homeless adults with alcohol use disorders.

NCT ID: NCT03673553 Completed - Pain Clinical Trials

The Multidisciplinary Treatment of Fibromyalgia.

Start date: January 31, 2016
Phase:
Study type: Observational [Patient Registry]

Background Fibromyalgia is a pathology characterised by chronic pain that harms people's quality of life. This pathology requires an MRT that combines pharmacological and non-pharmacological treatments. Currently, FPAs are important to society not only by offering activities that improve fibromyalgia symptomatology but also by increasing public awareness of the disease. The present study compares the effectiveness of a multimodal rehabilitation treatment (MRT) with that of the activities of a fibromyalgia patient association (FPA), and identifies the patient characteristics that can interfere with the success of interventions. Methods The quasi-experimental study selected forty-six older adults with fibromyalgia. The intervention group (n = 23) received pharmacological treatment, physical exercise, education, psychological therapies and Caycedian sophrology, while the control group (n = 23) carried out group psychological sessions and handicraft-based activities. Data collection included sociodemographic measures and responses to the Fibromyalgia Impact Questionnaire (FIQ). Participants were assessed pre- and post-intervention.

NCT ID: NCT03488641 Completed - Clinical trials for Hematologic Diseases

Systematic and Mechanism-based Approach to Rational Treatment Trials of Blood Cancer

SMART
Start date: April 16, 2018
Phase:
Study type: Observational

This observational study evaluates if drug response testing can be performed within 7 days and analyzes the value of ex-vivo drug screening for hematological malignancies as a biomarker to predict outcome, clinical course and response to treatment.

NCT ID: NCT03439930 Completed - Treatment Clinical Trials

The Effect of Balance Training on Neuromuscular Control in Subjects With CAI

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The goal of this study is evaluate the effect of uni-axial versus multidirectional balance training on muscle reaction time in subjects with chronic ankle instability. Muscle reaction time is measured on a trapdoor simulating an inversion sprain before and after a 6 week lasting balance training protocol.

NCT ID: NCT03375424 Recruiting - Clinical trials for Inflammatory Bowel Diseases

Vedolizumab Study With Inflammatory Bowel Disease Patients in Germany

VEDOibdI
Start date: October 2, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This study on biologics (Vedolizumab/anti-TNF) in the treatment of inflammatory bowel disease (IBD) patients in Germany extends the prospective documentation of efficacy in induction and maintenance therapy of anti-TNF to the use of Vedolizumab with a particular interest in the construction of a multifactorial model to predict long-term responses and favorable disease outcome or to predict severe side effects caused by therapy with biologics. Little data are available on the efficacy and safety of biologics in Germany in a real world situation. While the increasing use of anti-TNF-alpha antibodies in IBD-patients the new therapy with Vedolizumab opens up new opportunities in IBD-therapy, it may also pose new options and problems in terms of efficacy and predictors of response and potential side effects.

NCT ID: NCT03365141 Recruiting - Vitiligo Clinical Trials

Efficacy of Intralesional Triamcinolone Injection in the Treatment of Vitiligo

Start date: November 14, 2017
Phase: N/A
Study type: Interventional

A randomized split-body pilot study was planned to confirm efficacy of intralesiona triamcinolone injection in patients with vitiligo

NCT ID: NCT03351842 Recruiting - Treatment Clinical Trials

Surgery With or Without Chemotherapy for Stage I NSCLC With Micropapillary Component ≥ 20%

Start date: September 1, 2017
Phase: Phase 2
Study type: Interventional

Randomized phase II trial aims to compare surgery with or without adjuvant chemotherapy in treating patients who are pathologically diagnosed as stage I lung adenocarcinoma with micropapillary component no less than 20%.

NCT ID: NCT03316651 Recruiting - Treatment Clinical Trials

Sequential Therapy With WLL/Inhaling GM-CSF for Autoimmune Pulmonary Alveolar Proteinosis

Start date: August 2016
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the effectiveness of the sequential therapy with whole lung Lavage (WLL)/inhaling granulocyte-macrophage colony stimulating factor, compared to WLL only, for adult patients with severe autoimmune pulmonary alveolar proteinosis in China over a two-year period.

NCT ID: NCT03138785 Active, not recruiting - Treatment Clinical Trials

UVX as an Adjuvant in the Treatment of Fungal Keratitis

Start date: January 1, 2015
Phase: N/A
Study type: Interventional

In this study, investigators want to find the effect of adjuvant collagen cross-linking in the treatment of fungal keratitis