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NCT ID: NCT05059080 Terminated - COVID-19 Clinical Trials

A Six-Month Follow-Up Study of Participants With Coronavirus Disease 2019 (COVID-19) Previously Enrolled in a RO7496998 (AT-527) Study

MEADOWSPRING
Start date: June 15, 2021
Phase:
Study type: Observational

This study will evaluate the long-term sequelae of COVID-19 in patients diagnosed with COVID-19 who previously enrolled in a RO7496998 (AT-527) study (i.e. parent study NCT04889040 [CV43043]), for approximately 6 months after the end of the parent study.

NCT ID: NCT05059028 Completed - Breastfeeding Clinical Trials

Effect of Oxytocin Massage and Music on Breastfeeding

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

The aim of this study is to examine the effect of oxytocin massage and music performed immediately after birth on breastfeeding.

NCT ID: NCT05058716 Recruiting - COVID-19 Clinical Trials

Assessment of Clinical Effects of Coenzyme Q10 Levels in COVID-19 Patients in Intensive Care Unit

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

The study will be done in Hacettepe University Anesthesiology and Reanimation Intensive Care Unit. The investigators will accept COVID-19 diagnosed or suspected patients to the ICU. In the first day of hospitalization and after that once a week, the investigators will take blood samples from the patients to evaluate Coenzyme q10 levels. Our hypothesis is that there is a relationship between low coenzyme q10 levels and poor clinical outcome.

NCT ID: NCT05058586 Completed - Clinical trials for Stroke, Cardiovascular

The Effects of Aerobic Exercise Training on Cardiorespiratory Fitness in Stroke Patients

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

Background: Aerobic exercise training has favorable effects on quality of life, motor recovery, and aerobic endurance after stroke. Objectives: In this study, the investigators aimed to explore the effects of anti-gravity treadmill gait training and underwater walking therapy on cardiorespiratory fitness in stroke survivors.

NCT ID: NCT05058573 Active, not recruiting - Clinical trials for Tension-Type Headache

Effcet of Temporomandibular Joint Disorder Relaxation and Myofacial Relaxation Techniques on Tension Headache

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

The aim of this course is to investigate the effect of temporomandibular joint relaxation and myofacial relaxation techniques on quality of life , Joint range of motion, headache, depression in individuals with tension type headache.

NCT ID: NCT05058495 Completed - Clinical trials for Breast Cancer Related Lymphedema

The Effect of Mobile Lymphedema Self-Care Support Program on Self-Care in Women With Breast Cancer-related Lymphedema

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

The aim of this randomized controlled study is to evaluate the effect of the mobile lymphedema self-care support program on self-care, quality of life and symptoms related to lymphedema in women with breast cancer-related lymphedema. H1: There is a difference between the Lymphedema Self-Care Scale mean score in women who develop lymphedema due to breast cancer, according to the use of the mobile lymphedema self-care support program. H2: There is a difference between the Lymphedema Quality of Life Scale average score in women who develop lymphedema due to breast cancer according to the status of using the mobile lymphedema self-care support program. H4: There is a difference between lymphedema arm circumference measurements according to the use of the mobile lymphedema self-care support program in women who develop lymphedema due to breast cancer. H5: In women who develop lymphedema due to breast cancer, there is a difference in the situation of experiencing symptoms related to lymphedema according to the use of the mobile lymphedema self-care support program.

NCT ID: NCT05058378 Recruiting - Inguinal Hernia Clinical Trials

Correlation Between Spinal Anesthesia and Perfusion Index

Start date: September 20, 2021
Phase:
Study type: Observational

Investigation of the correlation between the success of obtaining unilateral spinal anesthesia and the measurement of perfusion index (pi).

NCT ID: NCT05058053 Completed - Phlebitis Clinical Trials

THE EFFECT OF COLD APPLICATION ON THE DEVELOPMENT OF PHLEBITIS IN PATIENTS RECEIVING INTRAVENOUS AMIODARONE TREATMENT.

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

This study, which has a quasi-experimental, prospective, and open-label randomized controlled design, was conducted to examine the effect of cold application on the development of phlebitis in patients receiving IV amiodarone infusion treatment. Study Hypotheses H0-1: There is no difference in the rate of development of phlebitis between the patients who received and who did not receive cold application during amiodarone IV infusion. H0-2: There is no difference in the grade of phlebitis between the patients who received and who did not receive cold application during amiodarone IV infusion. H0-3: There is no difference in the time of development of phlebitis between the patients who received and who did not receive cold application during amiodarone IV infusion.

NCT ID: NCT05057871 Completed - Shoulder Pain Clinical Trials

Efficacy of Pulse Electromagnetic Field Therapy (PEMF) in Patients With Subacromial Impingement Syndrome

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

The aim of our study is to investigate the effectiveness of Pulse Electromagnetic Field Therapy (PEMT) versus placebo on pain, quality of life, shoulder function and isokinetic assessment, and muscle strength in the treatment of subacromial impingement syndrome.

NCT ID: NCT05057585 Completed - Pain Clinical Trials

The Effects of Bed Exercises on Anxiety, Pain, Early Ambulation and Mobilization in Patients Undergoing Major Surgery

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

In this study, the effects of bed exercises on pain, anxiety, early ambulation and mobilization in major surgery patients were aimed. The research was experimental and a total of 120 patients participated. Data were collected using an information form, anxiety scale, and pain scale. Exercise was applied to the patients in the experimental group (15 minutes) and no intervention was applied to the control group. Descriptive statistics, correlation tests and t-test were used. Cronbach's alpha coefficients were checked for the scales.