Clinical trials

11

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

Condition / disease
Location
Status: Recruiting

Dental Caries and Oral Hygiene Status in Children With Specific Learning Disabilities

This study aims to evaluate dental caries and oral hygiene status in children aged 7-12 years with specific learning disabilities (SLD) and to compare the findings with healthy children. Clinical oral examinations, including dmft/DMFT, ICDAS II, Plaque Index, and Gingival Index assessments, will be performed. In addition, questionnaire-based evaluations of oral hygiene habits, dietary habits, and parental supervision during toothbrushing will be conducted.

Participants needed: 70
Trial details
Age: 7-12Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Children aged 7-12 years [+3]

Children with additional psychiatric diagnoses (e.g., autism spectrum disorder,... [+1]

Status: Recruiting

Plaque Removal Efficiency in Children With Specific Learning Disabilities

This study aims to evaluate the effectiveness of toothbrushing education on plaque removal in children aged 7-12 years with specific learning disabilities (SLD) and to compare their plaque removal performance with healthy children. Participants will receive standardized toothbrushing education supported by visual and auditory materials. Plaque Index, Gingival Index, and photograph-based quantitative plaque analyses will be evaluated at baseline and after a 2-week follow-up period.

Participants needed: 70
Trial details
Age: 7-12Biological sex: AllType: InterventionalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Diagnosis of specific learning disabilities confirmed by a child and adolescent... [+3]

Children with additional psychiatric diagnoses such as autism spectrum disorder,... [+1]

Status: Not yet recruiting

General Well-being After Quitting Drug Use

The aim of this study is to investigate physical and physicosocial well-being after quitting drug use.

Participants needed: 120
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Jun 11, 2026
Eligibility criteria

Active drug users and those using psychotic drugs

Status: Recruiting

Effect of Lemon Juice and Apple Cider Vinegar on Postprandial Blood Glucose and Satiety in Healthy Individuals

This clinical study aims to examine how acidic drinks (lemon juice and apple cider vinegar) affect blood sugar when consumed with a starchy food. The study focuses on healthy individuals and aims to understand whether these drinks can slow the rise in blood sugar after meals and affect feelings of fullness. The main questions this study aims to answer are: Do lemon juice or apple cider vinegar lower the rise in blood sugar after a meal? Do these drinks increase feelings of fullness? Do different amounts change their effects? Researchers will compare lemon juice and apple cider vinegar to see which one is more effective. Participants will: Consume white bread in the morning on an empty stomach with one of the following drinks: Water only Water with lemon juice (50 g or 100 g) Water with apple cider vinegar (10 g or 20 g) Have a one-week break between each test. Have their blood sugar measured at regular intervals for 3 hours after eating. Report their level of fullness using a simple scale. This study explores whether simple and practical dietary choices can help manage blood sugar levels. The findings may support new, easy-to-apply nutrition strategies for managing diabetes and weight.

Participants needed: 15
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: May 4, 2026Locations: 1
Eligibility criteria

Healthy male and female volunteers aged 18-35 years [+4]

Presence of any chronic disease (e.g., diabetes mellitus, cardiovascular disease... [+10]

Status: Recruiting

Effects of Graded Motor Imagery in Individuals With Foot/Ankle Osteoarthritis

The aim of our study is to evaluate the effects of graded motor imagery training applied in addition to a structured exercise program in individuals with foot and/or ankle osteoarthritis. The study population will consist of twenty-four individuals diagnosed with foot/ankle osteoarthritis who applied to the Orthopedics and Traumatology Department of Alanya Alaaddin Keykubat University Education and Research Hospital. Individuals who volunteer to participate in the study will be invited to participate through face-to-face interviews. The inclusion and exclusion criteria are as follows: Inclusion criteria: * Being 18 years of age or older * Having a diagnosis of foot/ankle osteoarthritis confirmed by a specialist physician through clinical and/or radiological examination * Experiencing pain in the ankle joint most days for at least three months * Agreeing to participate in randomly assigned treatment and follow-up measurements * Having a sufficient level of Turkish language comprehension * Having a Standardized Mini Mental Test score of at least 24 points Exclusion criteria: * Previous arthrodesis or joint replacement surgery on the affected ankle * Physical therapy for ankle osteoarthritis within the last three months * Vision or hearing problems that would affect compliance with treatment. * Presence of a neuromuscular disease * History of intra-articular ankle injections within the last 3 months * Initiation of a new disease-specific pharmacological treatment during the study period During the study period, participants will receive one of the physical therapy programs. One group will only participate in the structured exercise program, while the other group will receive graded motor imagery training in addition to the exercise program.Both treatment groups will receive a total of 12 treatment sessions over 6 weeks. The results of this study may help improve physiotherapy programs for individuals with similar health conditions.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Feb 18, 2026Locations: 2
Eligibility criteria

Be 18 years of age or older, [+5]

Previous arthrodesis or joint replacement surgery on the affected ankle, [+5]

Status: Not yet recruiting

Craniocervical Dysfunction Index in Patients With Temporomandibular Joint Dysfunction

The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with Temporomandibular Joint Dysfunction, reliability and validity of the index Turkish speaking adults.

Participants needed: 50
Trial details
Age: 20-60Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Feb 11, 2025Locations: 1
Eligibility criteria

Between the ages of 20-60 years [+3]

Over 60 years of age [+1]

Status: Not yet recruiting

Craniocervical Dysfunction Index in Turkish Patients With Non-specific Neck Pain

The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with non-specific neck pain, reliability and validity of the index Turkish speaking adults.

Participants needed: 50
Trial details
Age: 20-60Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Oct 15, 2024Locations: 1
Eligibility criteria

Between the ages of 20-60 years [+3]

Over 60 years of age [+1]

Status: Recruiting

Turkish Version of Digital Eye Strain Questionnaire (DESQ)

The aims of this study were to perform cultural adaptation of the DESQ and provide information regarding the factor structure, reliability and validity of the instrument in Turkish speaking adults.

Participants needed: 130
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Oct 15, 2024Locations: 1
Eligibility criteria

Between the ages of 18-65 years [+1]

History of ophthalmic surgery or active ocular disease [+1]

Status: Not yet recruiting

The Dubousset Functional Test in Total Knee Arthloplasty

The aim of this study is to investigate the validity and reliability of Dubousset Functional Test in the patients with Total Knee Prothesis.

Participants needed: 60
Trial details
Age: 50-70Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Oct 9, 2024
Eligibility criteria

Patients who had Total Knee Arthroplasty [+1]

Patients who didn't have any Total Kne arthroplasty [+1]

Status: Not yet recruiting

The Dubousset Functional Test in Lumbar Spinal Stenosis

The aim of this study is to investigate the validity and reliability of Dubousset Functional Test in the patients with lumbar spinal stenosis.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Oct 4, 2024
Eligibility criteria

Patients aged 18-65 years, diagnosed with chronic pain (more than three months)...

Those with fractures, pregnancy, a disease that would prevent physical exertion,...

Status: Recruiting

The Relationship Between Pes Planus, Diaphragm, Postural Control, and Plantar Pressure

Our primary aim is to compare diaphragm function (resting thickness, activity/resting thickness ratio indicating contractility), postural control, and plantar pressure between individuals with pes planus and healthy controls without pes planus.

Participants needed: 34
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Alanya Alaaddin Keykubat UniversityUpdated: Jul 9, 2024Locations: 1
Eligibility criteria

Willing to participate in the study voluntarily [+4]

Termination of voluntariness [+13]