Clinical trials

7

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Scapulothoracic Stabilization and Postural Training in Upper Extremity Lymphedema

This single-center randomized controlled trial aims to investigate the effects of adding scapulothoracic stabilization and postural training to standard lymphedema care in women with secondary upper extremity lymphedema following breast cancer surgery. Participants will be randomly assigned to receive either standard lymphedema care alone or standard care combined with scapulothoracic stabilization and postural training. Outcomes including scapular muscle strength, posture, upper extremity function, limb volume, and neck awareness will be assessed at baseline, immediately after treatment, and at a 2-month follow-up. The findings are expected to provide evidence regarding the effectiveness of incorporating targeted stabilization and postural exercises into conventional lymphedema rehabilitation.

Participants needed: 60
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Toros UniversityUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Female patients aged 18 to 65 years. [+3]

Active infection (e.g., cellulitis or lymphangitis). [+5]

Status: Recruiting

Respiratory and Relaxation Training in Lower Extremity Lymphedema

This randomized controlled trial aims to investigate the effectiveness of respiratory and relaxation training added to standard complex decongestive therapy (CDT) on muscle oxygenation, functional capacity, and limb volume in patients with lower extremity lymphedema. Participants will be randomly assigned to receive either standard CDT alone or CDT combined with respiratory and relaxation exercises. Outcomes will be assessed before treatment, immediately after treatment, and two months after completion.

Participants needed: 60
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Toros UniversityUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Female patients aged 18 years or older. [+4]

Acute cellulitis or other active infection within the previous 2-4 weeks. [+5]

Status: Not yet recruiting

Evaluation of Metabolic Parameters, Intestinal Permeability and Gastrointestinal Symptoms After Bariatric Surgery in Body Weight Management

This study aims to evaluate the changes in metabolic parameters, intestinal permeability, and gastrointestinal symptoms in individuals who have undergone bariatric surgery (Laparoscopic Sleeve Gastrectomy - LSG) for obesity treatment. Obesity is a chronic disease associated with serious health complications including type 2 diabetes, hypertension, cardiovascular disease, and metabolic disorders. Bariatric surgery is currently the most effective treatment method for morbid obesity. However, monitoring patients after surgery in terms of metabolic health, gut permeability, and gastrointestinal symptoms is crucial for long-term success. In this study, 40 volunteers (aged 19-50) who have undergone LSG surgery within the last month will be followed for 6 months. At the beginning of the study and 6 months later, the following will be assessed: * Metabolic parameters: fasting blood glucose, total cholesterol, triglycerides, high-density lipoprotein (HDL), low-density lipoprotein (LDL), very low-density lipoprotein (VLDL) cholesterol, and insulin levels * Intestinal permeability markers: zonulin, secretory immunoglobulin A (IgA), and lipopolysaccharide (LPS) levels * Gastrointestinal symptoms: assessed using the Gastrointestinal Symptom Rating Scale (GSRS) * Anthropometric measurements: body weight, height, waist and hip circumference, BMI * Nutritional intake: 3-day dietary records The study will be conducted at Bursa Yıldırım Doruk Hospital, General Surgery Clinic. Results will contribute to understanding the relationship between bariatric surgery and gut health, potentially helping to prevent postoperative complications.

Participants needed: 40
Trial details
Age: 19-50Biological sex: AllType: ObservationalSponsor: Toros UniversityUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Underwent Laparoscopic Sleeve Gastrectomy (LSG) within the last 1 month [+4]

Did not undergo or is not planned to undergo LSG [+7]

Status: Not yet recruiting

Turkish Validation of the ALOC Screening Scale in Older Adults

As the elderly population increases, health problems related to aging are also increasing. Loss of appetite negatively affects public health by causing malnutrition and related health problems in elderly individuals. Loss of appetite is a common problem in older adults, both in individuals with and without cognitive impairment. This can lead to serious health problems such as malnutrition, weight loss, muscle loss, weakening of the immune system and decreased quality of life. Cognitive disorders such as Alzheimer's and dementia can trigger loss of appetite, or loss of appetite can be a symptom of these disorders. Factors such as metabolic changes during the aging process, decreased sense of taste and smell, loneliness and depression contribute to loss of appetite. However, there is no valid and reliable scale in Turkey for the early diagnosis and assessment of loss of appetite. A scale being valid and reliable means that it can measure the concept it is intended to measure accurately and consistently. The aim of this study was to determine the validity and reliability of the Turkish version of the Loss of Appetite Scale in older adults with and without cognitive impairment .

Participants needed: 300
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Toros UniversityUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Elderly over 65 years, with or without cognitive impairment

Status: Not yet recruiting

Cancer Awareness Among Syrian Migrants

This study aims to develop and evaluate a theory-based educational intervention to improve cancer screening participation among Syrian migrants in Turkey. The study will also develop a Cancer Protection Motivation Scale (CPMS) to measure individuals' motivation toward cancer screening. Using a mixed-methods design, the study will explore barriers, beliefs, and behaviors related to breast, cervical, and colorectal cancer screening. The effectiveness of the intervention will be assessed using a pretest-posttest design. The findings are expected to support culturally appropriate strategies to improve cancer screening uptake among migrant populations.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Toros UniversityUpdated: Apr 24, 2026
Eligibility criteria

over 18 years of age [+4]

if they hold Turkish citizenship [+3]

Status: Not yet recruiting

Intravenous Catheter Application

The study was a randomised controlled trial showing the effect of watching cartoons and squeezing a stress ball on pain and fear in children admitted for intravenous catheter insertion. Hypotheses of the Study Hypothesis 1: Children who watch cartoons during intravenous catheter insertion have lower pain and fear scores than the control group. Hypothesis 2: The pain and fear of children who squeeze a stress ball during intravenous catheter insertion are lower than the control group Hypothesis 3: There is a difference between the pain and fear scores of children who watch cartoons and squeeze a stress ball.

Participants needed: 90
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: Toros UniversityUpdated: Aug 27, 2025
Eligibility criteria

Those who were admitted to Toros State Hospital, Child service on 01 September 2... [+5]

Children who cannot speak or communicate in Turkish, [+2]

Status: Recruiting

Effect of Dual-Task Training and Cognitive Rehabilitation in Individuals With Multiple Sclerosis.

The purpose of this study is to examine the effects of dual-task training and cognitive rehabilitation on gait, balance, fatigue and cognitive performance in individuals with multiple sclerosis.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Toros UniversityUpdated: Apr 29, 2025Locations: 1
Eligibility criteria

Definite MS diagnosis by a neurologist [+4]

Scoring 26 or below on the Montreal Cognitive Assessment Scale (MoCA) [+2]