Clinical Trials Logo

Anxiety State clinical trials

View clinical trials related to Anxiety State.

Filter by:

NCT ID: NCT05380661 Not yet recruiting - Clinical trials for Spinal Cord Injuries

Heart Rate Variability and Anxiety During Urinary Bladder Catheterization

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

This is a prospective, randomised study investigating the physical and psychological experience of intermittent catherization in adult individuals following spinal cord injury (SCI).

NCT ID: NCT05316415 Completed - Sleep Quality Clinical Trials

The Effects of Music on the Anxiety and Sleep Quality of Pregnant Women on Bed Rest for a High-risk Pregnancy

Start date: September 15, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to identify the effects of music on the anxiety and sleep quality of women with high-risk pregnancy having bed rest in the hospital in Turkey. This randomized-controlled study involved 80 control and 80 experimental group with a high-risk pregnant woman .

NCT ID: NCT05276505 Recruiting - Breast Cancer Clinical Trials

Aromatherapy Methods in Reducing Anxiety Before Breast Biopsy

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

A breast biopsy is a cause for anxiety for most women when faced with a diagnosis of breast cancer. Physiological and psychological effects of breast biopsy may continue in the pre-biopsy and post-biopsy period. The aim of this study is to compare the effectiveness of two different aromatherapy methods applied in reducing anxiety before breast biopsy.

NCT ID: NCT05253664 Completed - Anxiety State Clinical Trials

Effect of Woman-Centered Care on Anxiety and Comfort Levels

Start date: February 11, 2019
Phase: N/A
Study type: Interventional

H1a: There is a statistically significant difference in anxiety levels between women who received woman-centered care in the early postpartum period and women who received standard care. H1b: There is a statistical difference in terms of comfort levels between women who received woman-centered care in the early postpartum period and women who received standard care. H0a: There is no statistically significant difference in anxiety levels between women who received woman-centered care in the early postpartum period and women who received standard care. H0b: There is no statistical difference in terms of comfort levels between women who receive female-centered care in the early postpartum period and women who receive standard care.

NCT ID: NCT05172076 Recruiting - Anxiety State Clinical Trials

COVID-19-associated Anxiety of Pregnant Women for Anomalies, Stillbirth and Preterm Labor-2

CAASP2
Start date: January 1, 2022
Phase:
Study type: Observational

Capture of anxiety for anomalies, stillbirth and preterm labor of pregnant women during COVID-19 pandemia

NCT ID: NCT05032885 Recruiting - Clinical trials for Respiratory Insufficiency

Early Physiotherapy in Covid Patients

Start date: April 4, 2021
Phase: N/A
Study type: Interventional

Based on the hypothesis that early physiotherapy in patients hospitalized for COVID-19 improves their functional capacity, perceived quality of life and decreases anxiety. Our main objective is to analyze the differences between groups with respect to functional deterioration, need for oxygen therapy and anxiety when implementing an early physiotherapy program. We propose a randomized clinical trial with two arms and single-center, to be developed in hospitalization units and intermediate respiratory care units (IRCU), with patients diagnosed with COVID. The sample will consist of an experimental group of 66 admitted patients with COVID-19 to whom an early physiotherapy program will be implemented from 48-72 hours after admission. The control group will be made up of another 66 admitted patients with COVID-19 who will receive the treatment according to the usual procedure of the hospital center. Sociodemographic and clinical variables will be collected, including: modified MMRC dyspnea scale, amount of oxygen therapy, MRC-SS, sit to stand test, hand grip, Tinetti, HADS anxiety and depression questionnaire, SF-12 quality of life questionnaire, clinical frailty scale (CFS) and FRAIL scale. Patients in both groups will be re-evaluated two months after hospital discharge with the above variables in addition to the PCFS post-COVID patient functional status scale. A basic descriptive analysis and logistic regression will be performed to determine the effect of the intervention.

NCT ID: NCT04967378 Completed - Clinical trials for Mild Cognitive Impairment

Homebound Elderly People Psychotherapeutic Intervention

HEPPI
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

This study aims to develop, implement, and assess the feasibility, acceptability, and preliminary efficacy of a 10-week structured and individualized cognitive-emotional intervention program for homebound older adults with Mild Cognitive Impairment (MCI) and with depressive and/or anxiety symptoms. Homebound Elderly People Psychotherapeutic Intervention (HEPPI) is designed to maintain or improve memory functioning, reduce depressive and/or anxiety symptoms, and help participants to compensate or adapt to impaired cognitive performance, improving their quality of life and their subjective perception of memory and health.

NCT ID: NCT04960371 Recruiting - Anxiety State Clinical Trials

Effects of Anxiety on Coronary Microcirculatory Function in Hypertensive Patients

Start date: June 28, 2018
Phase:
Study type: Observational

This study assessed anxiety status and coronary flow reserve in hypertensive patients to investigate the effects of anxiety on coronary microcirculatory function.

NCT ID: NCT04924634 Completed - Depression Clinical Trials

Stress Levels and Mental Well-Being Among Slovak Students During e-Learning

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

Introducing restrictions on human contact has been effective in preventing the uncontrolled spread of COVID-19, however, it appears to have negatively impacted mental health. Psychological problems in different age groups occur with different intensity and duration of the pandemic. This study was aimed to assess the impact of introducing distance learning (e-Learning) on the stress levels and mental well-being among Slovak Students.

NCT ID: NCT04847362 Recruiting - Clinical trials for Postpartum Depression

The Effect of Tele-Health Education Provided in the Postpartum Period in the Covid 19 Pandemic

Start date: April 11, 2021
Phase: N/A
Study type: Interventional

In the planned study, it was aimed to examine the effect of tele-education offered in the postpartum period in the covid 19 pandemic on the levels of depression, attachment and anxiety of women.