Clinical Trials Logo

Filter by:
NCT ID: NCT05236244 Completed - Health, Subjective Clinical Trials

Motor Imagery in Healthy Individuals

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The research will be the first to examine the relationship between mental fatigue induced by motor imagery and upper extremity performance. This study, it is aimed to examine whether the effects of mental fatigue created by motor imagery on upper extremity performance can be reduced by diaphragmatic breathing exercises.

NCT ID: NCT05236140 Recruiting - Clinical trials for Electrical Stimulation

Electrical Stimulation in Men With Urinary Incontinence After Radical Prostatectomy

Start date: January 23, 2022
Phase: N/A
Study type: Interventional

Aim: In this study, the investigators aimed to assess the efficacy of perineal electrical stimulation on anxiety, depression, quality of life (QOL), and clinical parameters associated with incontinence in men with urinary incontinence after radical prostatectomy. Methods: This study is a prospective, randomized controlled trial. The investigators will recruit men who will be referred to the Urogynecological Rehabilitation Unit from other related outpatient clinics with complaints of urinary incontinence after radical prostatectomy. By using a random number generator, men will be randomized into two groups: as follows: perineal electrical stimulation (Group 1), and a control group. A random allocation sequence will be generated at a 1:1 ratio. The primary outcome measure is the continence rates, according to the literature. Furthermore, the severity of incontinence, incontinence episodes, social activity, anxiety, depression as well as QoL were secondary outcome measures. The 24-hour pad test will be carried out to evaluate the severity of incontinence. The Quality of Life-Incontinence Impact Questionnaire (IIQ7) will use to assess specific QoL related to incontinence. The Social Activity Index (SAI) contains, a 10-cm visual analog scale in which men may have problems with participation in social activities (0, impossible to participate;10, no problem to participate) will be used. The Hospital Anxiety and Depression scale (HADS) will use to evaluate the anxiety and depressive symptoms in men with UI after RP in the present study. In addition, treatment satisfaction will be evaluated. Men will evaluate the change in their urinary incontinence on a 5-point Likert scale (5, very satisfied; 1, very unsatisfied)

NCT ID: NCT05236101 Completed - Dental Anxiety Clinical Trials

Validation of Child Drawing Hospital Scale (CD: H) and the Place of the Drawing in the Evaluation of Dental Anxiety

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

Objectives: Our study aimed to perform a Turkish validation study of the Child Drawing: Hospital (CD:H) Scale and evaluate the dental anxiety and pain experienced during the treatment by drawing. Study Design: Pediatric patients between the ages of 4-13 who applied to the Pediatric Dentistry Department between 2018-2020 were included in the study. Following the translation of the CD:H Scale into Turkish and linguistic-cultural validation, the behaviors of pediatric patients during treatment were evaluated with the Frankl Behavior Rating Scale, the pain they experienced during treatment with the Wong- Baker Face Rating Scale, and their anxiety levels were evaluated with the pictures drawn by the patients at the end of the treatment. The data were analyzed with Statistical Package for the Social Sciences v23, and the significance level was taken as p <0.05. Results: Within the scope of the scale's reliability-validity study, the Intra-Class Correlation Coefficient (ICC) was evaluated with test-retest consistency. For section A,B,C and total score reliability was found to be positive and strong level correlation. Dental anxiety of boys was higher than girls. Conclusions: The Turkish version of the CD:H Scale is a reliable and valid scale that can be used to evaluate the dental anxiety of Turkish pediatric patients.

NCT ID: NCT05235997 Recruiting - Wrinkle Clinical Trials

Placebo Controlled Efficacy Evaluation of the Hydrolyzed Collagen Peptide In Adult Females

Start date: January 31, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the contribution of hydrolized collagen products to elasticity, hydration and roughness of the skin of female volunteers. Safety and tolerability of the product is the other objective of this placebo-controlled, randomized study.

NCT ID: NCT05235893 Completed - Analgesia Clinical Trials

Effect of Reflexology on Pain Management in Newborns

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

Introduction: Approximately 10-14 painful procedures per day are performed in preterm and term infants during the hospital stay in the first week. The investigators aimed to determine the effect of reflexology being applied to the sole during painful procedures on pain perception, behavioral responses, and physiological changes in newborns compared with other non-pharmacological methods. Material and Method: This study was planned as a randomized controlled trial in term infants being followed up in the Neonatal Intensive Care Unit (NICU) and maternity ward. To reduce pain during attempts to collect venous blood or heel lance which are routinely applied to term newborns before discharge; reflexology on the soles of the foot, 24% sucrose solution, kangaroo care, listening to classical music were applied to the babies and were compared to those who did not have any analgesic method.

NCT ID: NCT05235880 Completed - Parkinson Disease Clinical Trials

Effects of Virtual Reality Based Games in Rehabilitation of Parkinson's Disease

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

The purpose of this study is to investigate the effects of virtual reality based games on upper extremities, trunk and cognitive functions in patients with Parkinson's Disease.

NCT ID: NCT05235841 Completed - Blood Pressure Clinical Trials

Effect of Acupressure on Blood Pressure, Heart Rate and Pain Severity

Start date: July 15, 2018
Phase: N/A
Study type: Interventional

Objective: The aim of this study was to evaluate the effect of acupressure applied before CA procedure on systolic and diastolic blood pressure, mean arterial pressure, pulse and pain intensity parameters after CA. Design: The study is a randomized controlled trial. Setting: The study occurred at Cardiology Service (CS) of a Training and Research Hospital in Turkey. Participants: One hundred patients whomet the research criteria.

NCT ID: NCT05235308 Completed - Pain, Chronic Clinical Trials

Predictive Factors on the Results of Epidural Adhesiolysis in Patient With Chronic Spinal Pain

Start date: February 15, 2022
Phase:
Study type: Observational

The primary aim of this exploratory study was to determine the demographic, clinical, and technical factors associated with treatment outcome, to create a better select treatment candidates.

NCT ID: NCT05235295 Completed - Pain, Chronic Clinical Trials

Fluoroscopic vs Ultrasound Guided Sacroiliac (SI) Joint Injection

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The investigators aimed to evaluate the effectiveness of intra-articular sacroiliac joint injection under fluoroscopy versus ultrasound guidance

NCT ID: NCT05234541 Active, not recruiting - Clinical trials for Upper Extremity Surgery

Measurement of Cut-off Perfusion Index Value in Infraclavicular Blocks

Start date: July 1, 2021
Phase:
Study type: Observational [Patient Registry]

To investigate the value of the cut-off perfusion index showing that the block is successful in infraclavicular blocks performed under ultrasound guidance.