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NCT ID: NCT06010459 Completed - Exercise Tolerance Clinical Trials

Reference Values for the Six-minute Pegboard and Ring Test in Healthy Adults in Turkey

Start date: November 4, 2021
Phase:
Study type: Observational

Supported or unsupported arm activities are widely used in all activities of daily living. 6 PBRT is a valid, reliable, useful, practical and easy-to-apply test that evaluates unassisted arm endurance in patients with COPD, asthmatics, and healthy individuals. Studies have recently been conducted showing reference values for 6 PBRT in various populations. 6 Normative values and reference range for PBRT are not available for various ethnicities, including the Turkish population. Therefore, this study aimed to find reference values for 6 PBRT in the Turkish young and middle-aged individuals.

NCT ID: NCT06010420 Completed - Clinical trials for Sports Physical Therapy

The Effect of Using Medial Longitudinal Arch Supported Insoles on Jumping in Young Football Players

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

In this study, it was aimed to determine the effect of pressing styles and insoles on jumping performances.

NCT ID: NCT06010407 Completed - Psychological Clinical Trials

Examining the Attitudes of Physiotherapists on Patient Psychology

Start date: September 1, 2023
Phase:
Study type: Observational

To examine the psychology methods used by physiotherapists on patient psychology and to investigate their attitudes about psychology education.

NCT ID: NCT06010394 Completed - Knee Osteoarthritis Clinical Trials

Control of Edema in the Knee in Patients With Knee Osteoarthritis

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

The aim of this study was to compare the effectiveness of exercise and classical massage in the control of knee edema in patients with knee osteoarthritis.

NCT ID: NCT06010264 Completed - Rotator Cuff Tears Clinical Trials

THE EFFECTS OF EARLY PERIOD KINESIOTAPE

Start date: July 6, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to the effects of kinesio tape application on pain, edema, range of motion and functionality . The main questions it aims to answer are: - Does kinesiotape application reduce pain and edema and improve quality of life in the early period in individuals undergoing arthroscopic rotator cuff repair? - Does kinesiotape application provide early restoration of functional activity level in individuals undergoing arthroscopic rotator cuff repair? Participants will receive kinesiotaping in addition to traditional physiotherapy programs. If there is a comparison group: Researchers will compare kinesiotape group, shamtape group and control group to see if kinesiotaping.

NCT ID: NCT06010069 Completed - Fragility Clinical Trials

The Relationship Between the Frequency of Intraoperative Hypothermia and Fragility Scores

Start date: November 30, 2022
Phase:
Study type: Observational

The goal of this observational study is to compare frequency of intraoperative hypothermia between fragilitly groups of eldery patients who underwent orthopedic surgical procedures. It aims to answer those questions: - İs there any difference between fragility groups in terms of hypothermia frequency during orthopedic surgical procedures? - Are there any other factors that influence the frequency of hypothermia such as age, body mass index, room temperature etc. ? Participants body temperature before anestesia application,and before surgery had started was measured and measurament was done during whole procedure. Measuraments had been done by tympanic thermometer.

NCT ID: NCT06009887 Completed - Pregnancy Related Clinical Trials

Motivational Interview in Primiparous Pregnants With Low Belief in Normal Birth

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

This study aims to determine the effect of motivational interviews made with primiparous pregnant women with low belief in normal birth on medical and natural birth belief. This randomized controlled study was conducted in a randomized controlled manner with a total of 148 pregnant women who applied to the obstetrics outpatient clinic of a hospital in eastern Turkey (74 trials, 74 controls). In the study, a total of four sessions of motivational interviews were conducted with the primiparous pregnant women in the experimental group, one week apart. No intervention was applied to the women in the control group. Research data Personal Information Form, Belief Scale for Normal Delivery (BSND) and Birth Beliefs (Natural and medical birth belief) Scale (BBS) were used. Descriptive statistics, Pearson's chi-square test, and dependent and independent t-test were used to analyze the data.

NCT ID: NCT06009822 Recruiting - Kinesiophobia Clinical Trials

Investigation of Kinesiophobia and Functional Status of Patients After MPFL Reconstruction

Start date: August 1, 2023
Phase:
Study type: Observational

Our aim in this study is to examine the functional and clinical results of patients who have undergone MPFL reconstruction at least 2 years after the operation. The presence of kinesiophobia of the patients will be evaluated and its relationship with functional outcomes will be examined.

NCT ID: NCT06009796 Completed - Clinical trials for Transverse Maxillary Deficiency

The Effects of Various Rapid Palatal Expansion Appliances on Dentoskeletal, Dentoalveolar, Nasal and Airway Resistance

Start date: November 11, 2022
Phase: N/A
Study type: Interventional

This study aims to evaluate the effects of dentoalveolar, dentoskeletal, nasal resistance, and airway changes by applying rapid palatal expansion appliances in patients with maxillary constriction and the post-pubertal growth spurt stage.

NCT ID: NCT06009666 Completed - Clinical trials for Lymphedema of Upper Arm

Elastographic and Ultrasonographic Evaluation of Patients With Breast Cancer Related Lymphedema

Start date: February 1, 2022
Phase:
Study type: Observational

The aim of this study is to evaluate the feasibility of shear-wave elastography for the diagnosis and staging of breast cancer related lymphedema by assessing the skin and subcutaneous tissues of the arm and forearm, which could serve as a reference standard and be more easily applicable in daily life; and to investigate the relationship between the patients' symptoms and elastographic measurements.