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Affective Symptoms clinical trials

View clinical trials related to Affective Symptoms.

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NCT ID: NCT05741281 Completed - Clinical trials for Social Functioning, Alexithymia and Sense of Coherence , Bipolar Disorders

The Effect of Physical Exercises Program on Social Functioning, Alexithymia and Sense of Coherence Among Patients With Bipolar Disorders

Start date: February 5, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to: Investigate the effect of applying physical exercises program on social functioning, alexithymia and sense of coherence among patients with bipolar disorders Research Hypotheses - Clients who participated in physical exercises program will exhibit better social functioning and sense of coherence than the control group. - Clients who participated in physical exercises program will exhibit less alexithymia than the control group.

NCT ID: NCT05662137 Completed - Schizophrenia Clinical Trials

The Effect of Recognition and Expression of Emotions Program Applied to Schizophrenia Patients

Start date: January 15, 2023
Phase: N/A
Study type: Interventional

As a result of the positive and negative symptoms that occur in schizophrenia, patients with schizophrenia may experience negative emotions more frequently than individuals with other mental problems. Since these emotions can trigger psychotic symptoms, there is a need to develop effective emotion regulation strategies to be applied to patients with schizophrenia. Aim: In this study, it was aimed to examine the effect of emotion recognition and expression program on alexithymia and emotion expression in patients with schizophrenia.

NCT ID: NCT05460806 Completed - Quality of Life Clinical Trials

The Effect of Aerobic Exercise in Alexithymic Individuals With Chronic Pain

Start date: July 12, 2022
Phase: N/A
Study type: Interventional

It was aimed to investigate the effect of aerobic exercise on pain, alexithymia level and quality of life in young alexithymic individuals with chronic pain. There is no study in the literature comparing the effectiveness of aerobic exercise on alexithymia and chronic pain. Since our study will be the first study to investigate the subject, we foresee that it is scientifically important and will shed light on future studies. In addition, it is planned to make national or international papers and publications after the study is completed.

NCT ID: NCT04681235 Completed - Stroke Clinical Trials

Virtual Reality Training Affects on Motor Functions and Mental Health in Stroke Patients

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

In our study, we tested the hypothesis of the safe effect applicability of motor training in the immersion high-tech polymodal VR system not only on the parameters of balance, gait, and motor status of the patient, but also on his cognitive functions and mental health in patients with a degree of disability no more than 3 points on a scale Rankin.

NCT ID: NCT04533308 Completed - Virtual Reality Clinical Trials

The Impact of Virtual Reality on the Emotional State of Patients With Aphasia During Rehabilitation.

Start date: August 20, 2020
Phase: N/A
Study type: Interventional

The aim of the study is to determine virtual reality (VR) impact during standard program of rehabilitation on emotional state of patients with aphasia.

NCT ID: NCT04320459 Completed - Clinical trials for Ankylosing Spondylitis

Alexithymia in Ankylosing Spondylitis

Start date: February 1, 2016
Phase:
Study type: Observational

The study included 55 patients having Ankylosing Spondylitis (AS) for at least 1 year diagnosed according to the ASAS classification criteria who presented to our hospital's outpatient clinic and 55 healthy subjects. Demographic data were recorded for 55 AS patients who were subsequently assessed using the BASMI (Bath Ankylosing Spondylitis Metrology Index) in terms of elasticity and spinal mobility as well as the BASFI (Bath Ankylosing Spondylitis Functional Index) to determine functional status, the BASDAI (Bath Ankylosing Spondylitis Disease Activity Index) to assess the disease activity and the ASQoL (Ankylosing Spondylitis Quality of Life Questionnaire) to evaluate quality of life. The Toronto Alexithymia Scale-20 (TAS-20) was used for assessment of alexithymia and Beck's Depression Inventory (BDI) for depression among patients.

NCT ID: NCT04048720 Completed - Behavior Problem Clinical Trials

Norwalk Feasibility Study

Start date: July 5, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is two-fold: 1) to examine the feasibility of the Drop-In model of Family Nurture Intervention (FNI); and 2) to collect pilot data concerning the mother's response to the Drop-In model of FNI and short term effects of participation. Feasibility of the Program will be measured through costs, staffing, space availability, and uptake. Participation in the Drop-In entails weekly visits for FNI. The investigators hypothesize that the Family Nurture Intervention will show feasibility through attendance and positive response to the Drop-In format. The investigators also expect the Family Nurture Intervention to improve mother's perceived well-being and mother-child emotional connection.

NCT ID: NCT03964545 Completed - Clinical trials for Emotional Disturbances

Neurofeedback in Adolescents With Emotion Dysregulation

EFPTest
Start date: May 14, 2018
Phase: N/A
Study type: Interventional

A treatment to improve emotion regulation is tested in young patients with trauma-related mental disorder. The Electrical FingerPrint (EFP) from the amygdala is used for presenting patients with feedback (i.e. neurofeedback) from the amygdala, a brain region which plays a critical role in emotion and mental disorder. Via feedback, patients learn to self-regulate the neural circuit of emotion.

NCT ID: NCT03908268 Completed - Behavior Problem Clinical Trials

Children's Learning Centers Group FNI

Start date: January 29, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of Family Nurture Intervention in a mother-child group setting with a Standard Children's Learning Center (CLC) Program for preschool-aged children (ages 2-4.5). This approach is based on creating emotional connection and establishing mother-child two-way regulation, which the investigators hypothesize affects early child development. Mothers and children will be engaged by Nurture Specialists in comforting and calming interactions to regulate each other physically-leading to an automatic calming response to contact with each other.

NCT ID: NCT03844308 Completed - Clinical trials for Burnout, Professional

Wellness Tool in Anesthesia Providers

Start date: January 15, 2019
Phase: N/A
Study type: Interventional

This study will examine the effects of Isha Kriya meditation on stress and burnout among healthcare providers.