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NCT ID: NCT04427410 Completed - Clinical trials for Postpartum Depression

The Relationship Between Oxytocin Level and Postpartum Depression

Start date: July 20, 2019
Phase:
Study type: Observational

There are studies in the literature that associate oxytocin level with postpartum depression. This study was carried out to investigate the relationship between oxytocin levels measured during pregnancy and postpartum depression symptoms.

NCT ID: NCT04426929 Completed - Clinical trials for Rotator Cuff Injuries

Effectiveness of Structured Closed Kinetic Chain and Video Based Game Exercise Program in Rotator Cuff Lesion

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

Rotator Cuff muscles are injured due to frequent use, repeated subacromial loadings and circulatory failure, traction, compression, contusion, subacromial abrasion, inflammation, injection and age-related degeneration, causing Rotator Cuff ruptures.Rotator Cuff treatment strategies vary according to the stage of the disease. While conservative treatment is preferred in Stage 1 and Stage 2 of Rotator Cuff injuries, surgical approaches are performed in stage 3. The most common conservative methods used in its treatment are corticosteroid injections, nonsteroidal anti-inflammatory drugs and physiotherapy methods. When the literature is examined, there is no consensus about physiotherapy methods among conservative treatment approaches. It is stated in the literature that there is no standard exercise protocol for Rotator Cuff rehabilitation and specific exercise programs are needed. In addition, the virtual reality treatment approach, the most common example of the use of technology in rehabilitation, has begun to take part in rehabilitation studies. The aim of the project is to examine the effectiveness of video-based game exercise therapy in individuals with Rotator Cuff rupture, to develop a new exercise protocol with closed kinetic chain exercises and to investigate the most effective treatment method for Rotator Cuff ruptures.

NCT ID: NCT04426864 Completed - Clinical trials for Fibromyalgia Syndrome

Efficacy of Different Types of Exercises in Women With Fibromyalgia Syndrome.

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

Objective: To demonstrate the most effective exercise intervention for women with fibromyalgia syndrome on the pain, quality of life, depression, and body composition through a comparative study of three types of exercise intervention: supervised aerobic plus stretching, supervised resistance plus stretching, and home-based stretching.

NCT ID: NCT04426799 Completed - Nursing Student Clinical Trials

Effectiveness of Lemon Essential Oil of Aromatherapy in Reducing Test Anxiety in Nursing Students

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

This study examines the effectiveness of lemon essential oil in reducing test anxiety in first-year nursing students.

NCT ID: NCT04426682 Completed - Surgery Clinical Trials

Incontinence Surgery and Urodynamics Parameters

Start date: January 1, 2015
Phase:
Study type: Observational

In patients who have previously had incontinence surgery due to stress incontinence (Midurethral slings (tvt, tot, etc.)), the symptoms may return in the following years and the patient can reapply with urinary incontinence. Urodynamic evaluation is important before stress incontinence surgery to confirm clinical diagnosis based on symptoms and findings and to determine the factors that may affect the effectiveness of surgery and the possibility of complications. Urodynamics evaluation is performed in the preoperative period in patients scheduled for incontinence. Urodynamics evaluation is performed again in patients who applied with post-operative recurrence due to surgery failure or different reasons. It is aimed to show whether there is a difference between the urodynamics parameters of these patients who were examined preoperatively and the urodynamics parameters examined in case of postoperative failure. Thus, the primary goal; to show which of these parameters has deterioration or if the surgical method is insufficient if it is within certain limits or urinary incontinence may recur.

NCT ID: NCT04425980 Completed - Clinical trials for Hemiplegia; Congenital

The Efficacy of Two Models of Intensive Upper Limb Training on Quality of Life in Children With Congenital Hemiplegia

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

This study compared the effectiveness of two-mode of activity-based upper limb rehabilitation (Modified Constraint-Induced Movement Therapy and Bimanual training) on health-related quality of life outcomes in school-aged children with cerebral palsy

NCT ID: NCT04425928 Completed - Vestibular Disorder Clinical Trials

Activity Treatment on Vestibular Rehabilitation

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

In this study it was aimed to investigate the effects of home treatment program based standard activity on dizziness, balance and daily life activity in patients with dizziness complaint originated from chronic unilateral peripheral vestibular disorder and compare to effects of exercise-based home rehabilitation program.

NCT ID: NCT04425811 Completed - Stroke Clinical Trials

The Effect of Kinesiological Taping Applied to the Tibialis Anterior Muscle on Gait Parameter in Stroke Patients

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

The effect of kinesiological taping applied to the tibialis anterior muscle on gait parameter in stroke patients: Sham controlled study

NCT ID: NCT04425525 Active, not recruiting - Outcome Measure Clinical Trials

The Functional Difficulties Questionnaire-shortened Version: Turkish Translation, Validity and Reliability Study.

Start date: November 1, 2018
Phase:
Study type: Observational [Patient Registry]

The Functional Difficulties Questionnaire-shortened version "(FDQ-s) is a unique questionnaire that aimed at evaluating the functional performance of the upper extremities and trunk following cardiothoracic surgery. Aim of this study is adaptation of the FDQ-s questionnaire to Turkish culture and study its psychometric properties, validity and reliability.

NCT ID: NCT04425096 Completed - Clinical trials for Skin to Skin Contact

The Effect of Skin to Skin Contact on Postpartum Hemorrhage, Pain And Breastfeeding

Start date: May 25, 2020
Phase: N/A
Study type: Interventional

The aim of this study was to determine the effect of postpartum hemorrhage, pain and onset of early breastfeeding so that the skin applied at the third stage of birth is in contact with the skin. Material and Method: The study was carried out as a randomized controlled single-blind experimental study. The sample consists of 68 healthy mother and baby pairs. Skin contact with mothers and babies in the experimental group will be applied for 34 minutes immediately after birth. Routine care will be applied to the babies in the control group. Data will be collected using Personal Information Form, Visual Analogue Scale, LATCH Breastfeeding Diagnostic Scale, Breastfeeding Self-Efficacy Scale, postpartum hemorrhage follow-up bag, pad and oxytocin, ᵦ endorphine analysis results. were collected using Personal Information Form, Visual Analogue Scale, LATCH Breastfeeding Diagnostic Scale, Breastfeeding Self-Efficacy Scale, postpartum bleeding follow-up bag, pad and oxytocin, ᵦ endorphin analysis results.