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NCT ID: NCT05074407 Completed - Neck Pain Clinical Trials

Neck Pain in Office Workers During Covid 19 Pandemic

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

Work content of office workers are using computers, conferences, presentations and talking on the phones. Static postures and repetitive writing and reading activities at inappropriate body postures are the most common activities of office workers. Decreased physical activity and prolonged computer use cause occupational safety problems and musculoskeletal problems. Neck pain is one of the most common problem in office workers and the studies have shown the incidence of neck pain in office workers is 34-49% . The aim of this study to evaluate the effects of remote employee in neck pain in Office workers during covid 19 pandemic

NCT ID: NCT05074004 Completed - Psychoeducation Clinical Trials

The Effect of Psychoeducation Given In Psychiatry Day Hospital

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

Background: Psychoeducation is a process used in the realization of the principles of treatment and rehabilitation of mental illnesses and aims to help the patient and his/her family outside the hospital, to help the patient cope with the problems, experiencing, and to support them to live productive lives in society. Aims: This study aims to determine the effect of psychoeducation, given in a psychiatry dayhospital, on patients' self-sufficiency and well-being. Methods: The research is a single-blind randomized controlled experimental study. The sample of the study consisted of 28 schizophrenic patient(14experiment-14control), who agreed to participate in the study, followed in XXX University Psychiatry Day Hospital. In the study, an 8-week psychoeducation program was applied to the experimental group, and no intervention was made tothe control group. Socio-demographic data form, self-sufficiency scale, and well-being scale were used as data collection tools. The data obtained were analyzed using theSPSS-23 package program. Results: After the eight-week psychoeducation program, the pretest and posttest scores of the evaluations obtained from the scales of both groups were compared. It was found that while there was no change in thescores of the control group, there was an increase in the well-being and self-efficacy scores of the experimental group. While the increase in well-being was statistically significant(p<0.05), the increase in self-sufficiency score wasnot statistically significant(p>0.05), but the numerical increase was considered tobe aclinically significant result.

NCT ID: NCT05073900 Completed - Clinical trials for Myofascial Pain Syndrome

Comparison of the Efficacy of Rhomboid Intercostal Block and Erector Spinal Plane Block on Myofascial Pain Syndrome

Start date: July 10, 2021
Phase: N/A
Study type: Interventional

The investigators evaluate the effect of Ultrasound guided Rhomboid Intercostal Block and Erector Spinal Plane Block on lower cervical and inter scapular Myofascial Pain

NCT ID: NCT05073887 Completed - Knee Pain Chronic Clinical Trials

A Comparison of Ultrasound Guided Genicular Nerve Blockade Using Current Versus Revised Anatomical Targets

Start date: March 10, 2021
Phase: N/A
Study type: Interventional

comparison of effectiveness of ultrasound guided genicular nerve blockades and radio frequency stimulation

NCT ID: NCT05073731 Recruiting - Multiple Sclerosis Clinical Trials

Telerehabilitation-based Upper Extremity Training in People With Multiple Sclerosis

Start date: December 15, 2021
Phase: N/A
Study type: Interventional

In this studly, the effects of an 8-week telerehabilitation-based upper extremity training in persons with multiple sclerosis will be investigated.

NCT ID: NCT05073497 Completed - Pain Clinical Trials

Efficacy of Finger Puppet as a Distraction Method

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

The study will be conducted with the randomized controlled experimental method. The children who attended the pediatric emergency department will divide into two groups via randomization in the computer environment. After the randomization, children in the experimental group will play with finger puppets under the direction of the researcher during venipuncture. On the other hand, no application will perform on the children in the control group during the venipuncture. The parents will also be found next to their children in both groups during the procedure.

NCT ID: NCT05073289 Completed - Anxiety Clinical Trials

Sandplay Activity in Psychiatry Clinic (SAPC)

Start date: February 27, 2020
Phase: N/A
Study type: Interventional

This research was conducted to examine the effect of sandplay activity on anxiety and well-being levels in patients in psychiatric clinics. The research was carried out in Isparta Süleyman Demirel University Psychiatric Clinic as a single-blind randomized controlled experimental study in the pre-test, final-test order between 2020-2021. Ethical permission was obtained from the Clinical Research Ethics Committee and application permission from the institution for pre-research. 63 patients (intervention-32 and control-31) selected by block randomization method formed the universe of the study. No intervention was applied to the control group. A preliminary test and a final test were performed two days apart, one hour apart on the first and fourth days. Two sessions of sandplay activity were applied to the intervention group with a decongest of two days, and each session was pre-tested. The data was collected using "The Personal Information Form", "The Spielberger Status Anxiety" inventory, and "Well-Being Star Scale" and also data showed normal distribution. In statistical analysis, T-Test, Chi-Square Test, pearson correlation test was used dependent and independent groups. For the purpose of the research, the hypotheses of the research are as follows:: 1. Hypothesis (H1): after intervention, anxiety levels of patients who underwent sandplay activity (in a psychiatric clinic) are lower than in the control grouproup 2. Hypothesis (H1): after intervention the level of well-being of patients undergoing sand play activity (in a psychiatric clinic) is higher than that of the control group. 3. Hypothesis (H1): there is a negative correlation between the level of anxiety and the level of well-being in psychiatric clinics who sandplay activity is practiced and not practiced. This research is Turkish language.

NCT ID: NCT05073198 Completed - Testicular Cancer Clinical Trials

The Effect of the Brochure on Testicular Self-Exam

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

This study aims to examine the effect of the educational brochure given to university students on testicular cancer and its early diagnosis on their health beliefs and self-examination; In non-randomized groups, pretest-posttest was conducted in a quasi-experimental design with control group. The research was carried out with students studying in the psychological counseling and guidance department of a state university in Turkey. The study group consisted of 92 students, 48 of which were experimental and 44 were control. Only the experimental group was given an educational brochure about testicular cancer and testicular self-examination. Data; Personal information form, testicular cancer and health beliefs scale about testicular self-examination were collected with the form for self-examination. In the evaluation of the data; Mann Whitney U, Wilcoxon and chi-square analyzes were performed.

NCT ID: NCT05073055 Completed - Postoperative Pain Clinical Trials

Spinal Anesthesia Versus Erector Spina Plane Block

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

The primary aim of our study was to use spinal anesthesia for unilateral inguinal hernia surgery and lumbar erector spina block supported by local infiltration anesthesia in terms of operation time, intraoperative hemodynamic data, motor block onset time, block termination time, analgesic need, discharge time, patient satisfaction, surgeon satisfaction. is to compare. Its second purpose is to observe nausea, vomiting, urinary retention, headache, chills, bleeding, wound infection.

NCT ID: NCT05073016 Completed - Healthy Clinical Trials

The Effect of Intermittent Theta Burst Stimulation on Motor Learning in Healthy Adults

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

This study investigates the effect of different application frequencies of intermittent theta burst stimulation on motor learning in healthy adults.