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NCT ID: NCT06142331 Completed - Home Exercise Clinical Trials

Applicability of Home-based Exercise Programs in Physiotherapy

Start date: November 17, 2023
Phase:
Study type: Observational [Patient Registry]

Aim: In this study, the types of home-based exercise programs prepared for patients receiving physiotherapy services in different rehabilitation institutions; It is aimed to examine the applicability and effectiveness advantages according to disease status, age, gender, socioeconomic level, education level, confidence in the home program, and functional independence level. Study type: observational study Research question; To what extent do patients participate in home-based exercise programs?

NCT ID: NCT06142110 Completed - Injury Clinical Trials

The Relationship Between Functional Movement and Respiratory Muscle Strength

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

Functional Movement Screen (FMS) is a battery used for injury prediction, identifying asymmetry and weak connections in basic functional movement patterns. The muscles assessed in FMS are also respiratory muscles. Therefore, FMS scores were thought to be related to respiratory muscle strength. The aim of our study was to examine the relationship between Functional Movement Screen and respiratory muscles strength in professional football players and sedentary individuals.

NCT ID: NCT06141863 Completed - Clinical trials for Temporomandibular Joint Dysfunction Syndrome

Temporomandibular Dysfunction in Patients With Cervical Disc Herniation

Start date: May 1, 2022
Phase:
Study type: Observational [Patient Registry]

Cervical spine problems are associated with temporomandibular joint (TMJ) and related muscles.The aim of the present study was to investigate temporomandibular joint dysfunction (TMD) and pain in individuals with cervical disc herniation (CDH) according to the level of neck disability.

NCT ID: NCT06141759 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

The Effect of Conservative Treatment on Perceptual and Cognitive Asymmetry in Scoliosis

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

Adolescent idiopathic scoliosis (AIS) patients have been found to exhibit cortical asymmetry. This study aimed to examine the impact of conservative treatments on perceptual and cognitive asymmetry in the auditory system assessed by dichotic listening in AIS patients with thoracic major curves.

NCT ID: NCT06141122 Completed - Clinical trials for Patient Satisfaction

The Colonoscopy Booklet:Effect of a Recipe Resource on Quality of Colonoscopy Bowel Preparation and Patient Experience

Start date: September 15, 2023
Phase: N/A
Study type: Interventional

This study aimed to provide a recipe resource with visuals in line with the low-residue diet recommendations given to patients before colonoscopy, including cooking instructions for the meals in the diet list. In this way, we aimed to minimize confusion regarding dietary restrictions during colonoscopy preparation and ensure full compliance with the diet list. Our hypothesis is that this approach may enhance compliance with current recommendations and improve the quality of bowel preparation.

NCT ID: NCT06139900 Completed - Healthy Clinical Trials

How Virtual Reality is Impacting Balance: An Examination of Postural Stability

Start date: April 2, 2021
Phase:
Study type: Observational

There are several studies examining the effects of different sensory stimuli on balance in healthy young people. Our study will especially explain how the same environment will affect postural control, when projected into VR environment. In this way, we aim to contribute to the literature and virtual reality programs used in rehabilitation.

NCT ID: NCT06139562 Completed - Obesity Clinical Trials

Two Different Dietary Approaches in Body Composition

Start date: September 27, 2019
Phase: N/A
Study type: Interventional

Objective: In this study, it was aimed to determine the effect of time-restricted feeding on anthropometric measurements and leptin, ghrelin, adiponectin, insulin and cortisol hormone levels in obese women. Material and Methods: This study was carried out with women who voluntarily accepted to participate in the study who applied to the Baskent University Ankara Hospital Endocrinonogy Outpatient Clinic between September 2019 and October 2020. Women between the ages of 20 and 50, with a body mass index of 29-35 kg/m2, without any chronic disease, who did not have a weight loss diet in the last 6 months, and who had regular night sleep were included in the study. This study was planned as a randomized cross-over design for a total of 9 weeks. Two different dietary interventions, "time-restricted feeding" and "extended-time feeding", were applied to 4 weeks for each group and a week for wash-out period. Anthropometric measurements and hormone levels of individuals were evaluated at the beginning and end of the study.

NCT ID: NCT06139445 Completed - Clinical trials for Manual Lymphatic Drainage Effects

Manual Lymphatic Drainage for Pain, Muscle Strength, and Sensation

Start date: November 8, 2023
Phase: N/A
Study type: Interventional

To evaluate the acute effect of MLD on pressure pain threshold (PPT), pain tolerance, tactile sensation, and muscle strength in healthy young adults. healthy young adults were included in the study. Before and after MLD and plasebo touchs, the same physiotherapist performed PPT and pain tolerance measurements, muscle strength measurements with a hand dynamometer (Jamar®) and pinchmeter (Baseline®), and two-point discrimination (2PD) evaluation with an esthesiometer.

NCT ID: NCT06139120 Completed - Clinical trials for Central Sensitisation

The Segmental Distribution of Hypersensitivity in Patients With Chronic Subacromial Pain Syndrome

Start date: September 20, 2022
Phase:
Study type: Observational [Patient Registry]

This study aimed to determine the distribution of pain sensitivity according to body segments in patients with central sensitization associated with chronic subacromial pain syndrome (SPS).This cross-sectional study included patients with chronic SPS and central sensitization (patient group) and the same number of healthy participants as controls. The presence of central sensitization was determined using the Central Sensitization Inventory. To determine the segmental distribution of pain sensitivity, pressure pain threshold measurements were performed bilaterally from the shoulder, forearm, and leg.

NCT ID: NCT06138938 Completed - Cesarean Section Clinical Trials

Effects of Abdominal Irrigation During Cesarean

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

This prospective randomized controlled clinical trial was conducted between March 2022 and May 2022 and included 60 patients who underwent elective cesarean. The participants were randomized into two groups: abdominal irrigation (n=30) and control group (n=30). Participants undergo a standard cesarean procedure, and general anesthesia was preferred. The patients were questioned regarding nausea, vomiting, highest pain scores, time of flatus, and stool passage during the postoperative period.