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NCT ID: NCT05777161 Completed - Anxiety Disorders Clinical Trials

A Trial of Parent-coached Exposure Therapy for Children With Anxiety Disorders and OCD

Start date: November 11, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effectiveness of parent coached exposure therapy (PCET) and standard cognitive behavioral therapy (CBT) in treating childhood anxiety disorders and obsessive compulsive disorder (OCD).

NCT ID: NCT05775653 Completed - Clinical trials for Chronic Conditions, Multiple

Group-based [ADAPT] Versus One-to-one [Usual] Occupational Therapy: A Pilot and Feasibility Study

Go:OT
Start date: March 27, 2023
Phase: N/A
Study type: Interventional

Background: The number of people living with chronic conditions limiting the ability to perform activities of daily living (ADL) tasks is increasing. Occupational therapists are trained to deliver interventions to improve ADL ability. Municipality occupational therapy interventions are usually delivered as one-to-one sessions in the client´s home. While this intervention format might be effective, a group-based intervention format might be as effective but more cost-effective? Hence, the group-based ADAPT program was developed, piloted and evaluated for its functioning and feasibility in municipality settings. These studies provided initial evidence for the ADAPT Programs effectiveness. A randomized controlled trial (RCT) is however needed to document effectiveness, processes, and cost-effectiveness of the ADAPT program versus usual occupational therapy (UOT) for people with chronic conditions. Prior to the RCT, this pilot and feasibility study will be conducted to test aspects of trial design, conduct and processes as well as intervention content and delivery. Material and Methods: A total of 16 home dwelling persons with chronic conditions, experiencing ADL task performance problems will be randomized and allocated to receive ADAPT (intervention) or UOT (control). Effectiveness and cost-effectiveness assessments are collected at baseline and post intervention i.e., 3-months (week 12) and 6-months (week 26) from baseline. Pilot and feasibility aspects will be evaluated by means of registrations forms filled out by the OTs delivering ADAPT and people with chronic conditions attending ADAPT. Registrations are designed to inform aspects of 1) recruitment and retention, 2) trial participation, 3) impact of trial on participants and staff, 4) completion rates, 5) fidelity and dose 6) assesable information and 7) adaptation of trial conduct to local context. Progression criteria for when to 'go', 'amend' or 'be alert/stop' are defined, to support the decision on whether to continue to RCT or the need to adjust design or procedures,

NCT ID: NCT05747911 Completed - Migraine Disorders Clinical Trials

Dietary Advanced Glycation End Products and Migraine

Start date: February 1, 2022
Phase:
Study type: Observational

Is dietary intake of advanced glycation different between individuals with and without migraine? Is there a difference between the groups in terms of energy and nutrients? The answers to these questions are sought.

NCT ID: NCT05740826 Completed - Clinical trials for Temporomandibular Joint Disorders

Correlation Between Cervical Spine Muscle Disorders and the Occurrence of Symptoms of Temporomandibular Joint Dysfunction

Start date: September 8, 2022
Phase:
Study type: Observational

This study evaluated the correlation between the occurrence of disorders of selected muscles of the cervical spine and the occurrence of symptoms of TMJ dysfunction

NCT ID: NCT05729828 Completed - Nurse's Role Clinical Trials

Psychometric Properties of the SMART Feeding Tool

Start date: May 5, 2021
Phase:
Study type: Observational

This observational study aims to evaluate the psychometric properties of a new infant feeding tool called "SMART Tool" in the neonatal intensive care unit. The main questions it aims to answer are: 1. To design a feeding tool to assess oral motor and neurobehavioral skills in neonates 2. To establish psychometrics of the new tool by doing reliability and validity tests.

NCT ID: NCT05718414 Completed - Clinical trials for Complication Following Peripheral Nerve Block (Diagnosis)

Artificial Intelligence for Ultrasound-Guided Peripheral Nerve and Plane Blocks

Start date: February 8, 2023
Phase:
Study type: Observational

The goal of this observational study is to test the accuracy of an artificial intelligence tool used for identifying ultrasound-guided block regions in healthy volunteer participants. The main question aims to answer is: • Is the artificial intelligence tool effective for identifying selected ultrasound-guided nerve block regions and their anatomical landmarks? Three anesthesiology trainees perform ultrasound scanning for 8 nerve block regions on participants. Peripheral nerve and plane block regions are; - Adductor canal block region - Axillary brachial plexus block region - ESP (erector spinae plane) block region - Femoral block region - PECS (pectoral) block region - Popliteal block region - Rectus sheath block region - Superficial cervical plexus block region

NCT ID: NCT05712655 Completed - Head Pain Clinical Trials

Masticatory Muscles Electromyography in Post-pubertal Females With Forward Head Posture and Temporomandibular Disorders

Start date: July 1, 2021
Phase:
Study type: Observational

The aim of this study was to evaluate masticatory muscle electrical activity in post-pubertal females with forward head posture (FHP) and temporomandibular disorders (TMD) as well as in post-pubertal females with neutral head posture and with no temporomandibular disorders.

NCT ID: NCT05712590 Completed - Body Composition Clinical Trials

The Influence of the Nutritional Status of Women Between 30 and 45 Years of Age on the Condition of the Skin and Body Composition

VEGOMNI
Start date: December 19, 2022
Phase:
Study type: Observational

Goal is to investigate the differences in skin condition and body composition among women with different dietary habits aged 30-45 years. Study will be focused onto sub-groups of female subjects following omnivorous, vegetarian or vegan diet.

NCT ID: NCT05695989 Completed - Clinical trials for Bariatric Surgery Candidate

Safety and Feasibility of the Use of the Dual Robotic Arm Accessory With the Levita Magnetic Surgical System in Laparoscopic Procedures

MARS GI
Start date: January 19, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and feasibility of the Levita Dual Robotic Arm Accessory (DRAA) used with the Levita Magnetic Surgical System (MSS)

NCT ID: NCT05693389 Completed - Bipolar Disorder Clinical Trials

Efficacy of Acceptance and Commitment Therapy on Impulsivity and Suicidality Among Clients With Bipolar Disorders

Start date: September 15, 2022
Phase: N/A
Study type: Interventional

Psychiatric nurses face a huge challenge in predicting and preventing suicide behaviour in their patients with bipolar disorders, but it may also be one of the most accurate measures of how well their clinical care is working. In addition to, high impulsivity scores are associated with increased overall functional impairment, a higher number of episodes with early onset, and a higher number of past suicide attempts, as well as increased substance intake. Thus, this study aimed at evaluating the efficacy acceptance and commitment therapy on impulsivity and suicidality among bipolar clients. research hypnosis - Clients who engaged in acceptance and commitment therapy had less impulsivity than the control group. - Clients who engaged in acceptance and commitment therapy had less suicidality than the control group.