Clinical trials

13

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Condition / disease
Location
Status: Recruiting

Peloid Therapy in Temporomandibular Joint Dysfunction

This prospective, single-group clinical study will evaluate whether local peloid therapy improves pain and jaw function in adults with temporomandibular joint dysfunction. Participants will receive peloid therapy applied to the temporomandibular joint region and masticatory muscles for 20 minutes per session, 5 days per week, for 2 weeks. Pain and functional outcomes will be measured at baseline and at the end of treatment using validated clinical scales, including the Jaw Functional Limitation Scale-8, visual analog scale pain scores, Fonseca index, maximum mouth opening, and secondary otalgia assessment.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Age between 18 and 65 years [+4]

History of temporomandibular joint trauma, tumor, active infection, or acute inf... [+6]

Status: Recruiting

Effects of Isotretinoin on Smell

Isotretinoin is a common medicine used to treat moderate to severe acne. It often causes dryness of the skin and the inside of the nose. Because a normal sense of smell depends on a healthy nasal lining, this dryness may affect how well a person can smell. This study will examine whether isotretinoin treatment changes the sense of smell in adults with acne. Before starting isotretinoin, participants will complete a standardized smell test and two short questionnaires about nasal symptoms and quality of life: the Nasal Obstruction Symptom Evaluation (NOSE) scale and the 22-item Sino-Nasal Outcome Test (SNOT-22). After at least 4 weeks of treatment, the same smell test and questionnaires will be repeated. By comparing results before and after treatment, the study will test the hypothesis that isotretinoin has a negative effect on olfactory function and may reduce patients' ability to smell.

Participants needed: 54
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Diagnosed with acne and scheduled to start oral isotretinoin as part of routine... [+4]

Younger than 18 years or older than 45 years [+4]

Status: Recruiting

Cognitive Reserve and Post-Fatigue Recovery in Older Adults

As people grow older, it is common to experience a drop in physical stamina and memory functions. This can make recovering from daily physical and mental fatigue more difficult, which directly impacts an individual's independent daily life and overall quality of life. "Cognitive reserve" is a term that describes the brain's built-in resilience. Built over a lifetime through education, work, and social activities, a higher cognitive reserve acts like a buffer, helping the brain adapt to stress and aging. While research shows that a high cognitive reserve protects against conditions like dementia, we still do not fully understand how it helps older adults bounce back from normal, everyday physical and mental exhaustion. The goal of this study is to investigate how cognitive reserve levels influence how individuals aged 65 and older perceive their recovery after experiencing physical and mental fatigue. What the Study Involves The researchers will evaluate participants aged 65 and older to measure their baseline cognitive reserve levels. The study will look closely at how these levels affect the participants': Ability to cope with daily physical and mental fatigue. Need for rest and rest patterns. Time and ability to return to normal daily activities. Overall perception of their mental and physical recovery. Expected Outcome By understanding this relationship, the study aims to fill a gap in medical literature and help healthcare providers design better, more personalized rehabilitation and lifestyle support programs to improve the quality of life for older adults.

Participants needed: 400
Trial details
Age: 65-90Biological sex: AllType: ObservationalSponsor: Uşak UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

being 65 years of age or older, [+1]

Being younger than 65 years old, [+2]

Status: Not yet recruiting

High-power Laser Therapy for Notalgia Paresthetica.

A non-invasive modality for the management of neuromusculoskeletal pain conditions that has emerged as a compelling option is high-power laser therapy (HPLT). The pathophysiology of notalgia paresthetica (NP) is treated uniquely by HPLT, which targets both the presumed muscular component of nerve entrapment and the resultant neuropathic symptoms. The main goal of this study, which is randomised, controlled and blinded by assessors, is to find out how well High-Power Laser Therapy (HPLT) works as an extra treatment to standard care in reducing itching, pain and improving quality of life for patients with long-term nerve pain.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jan 23, 2026
Eligibility criteria

Adults aged 18-75 years [+4]

- Secondary causes of symptoms (e.g., spinal pathology, herpes zoster, renal fai... [+6]

Status: Recruiting

The Efficacy of High-Power Laser Therapy in Meralgia Paresthetica

The management of MP typically follows a conservative pathway, encompassing patient education, lifestyle modifications (e.g., avoidance of tight garments, weight loss), pharmacotherapy (such as neuropathic pain agents or corticosteroid injections), and physical therapy. However, evidence supporting the efficacy of these interventions is largely anecdotal or derived from low-quality studies, and a substantial proportion of patients experience persistent symptoms refractory to standard care. Therefore, the primary objective of this randomized, sham-controlled, assessor-blinded study is to investigate the efficacy of HPLT as an adjunct to standard conservative care on pain intensity, sensory symptoms, and functional capacity in patients with chronic Meralgia Paresthetica. The investigators hypothesize that patients receiving active HPLT will demonstrate significantly greater improvements in these outcomes compared to those receiving a sham laser procedure

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jan 13, 2026Locations: 1
Eligibility criteria

Adults aged 18-65 years. [+3]

Secondary MP (e.g., due to pelvic surgery, trauma, or tumor mass effect confirme... [+6]

Status: Recruiting

Inspiratory Muscle Training After Stroke

Objective: To investigate and compare the efficacy of a 6-week, supervised respiratory training program using the AiroFit PRO™ mobile respiratory trainer against traditional Pursed-Lips Breathing exercises in individuals with hemiplegia. Study Design: A single-blind, two-arm, randomized controlled trial. Participants: Ambulatory adults with stable hemiplegia (≥3 months post-stroke), who are medically stable and able to follow commands. Interventions: Participants will be randomly assigned to one of two groups: Experimental Group: Will perform Inspiratory Muscle Training using the AiroFit PRO™ device for 15 minutes/day, 5 days/week, for 6 weeks. The intensity will be progressively increased. Active Control Group: Will perform Pursed-Lips Breathing exercises for an identical duration and frequency. Primary Outcomes: Changes in pulmonary function tests, including Forced Vital Capacity (FVC), Forced Expiratory Volume in 1 second (FEV1), and Maximal Inspiratory Pressure (MIP). Significance: This study will provide high-level evidence on the utility of smart, device-guided respiratory training as a novel component of neurorehabilitation, potentially offering a more effective strategy to improve respiratory health and overall recovery in hemiplegic patients compared to standard breathing exercises.

Participants needed: 54
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

Clinical Diagnosis: A confirmed diagnosis of unilateral hemiplegia or hemiparesi... [+4]

Pre-existing, significant respiratory diseases (e.g., severe COPD, asthma, pulmo... [+3]

Status: Recruiting

The Effect of Graded Forced Expiration on Intraocular Pressure

The primary objective of this study is to utilize the Airofit device to systematically measure and characterize the changes in intraocular pressure across its six different levels of forced expiration. This investigation will provide crucial quantitative data on the IOP-respiratory effort relationship, enhancing our understanding of IOP dynamics during controlled respiratory stress and establishing a new, standardized paradigm for such research.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Dec 22, 2025Locations: 1
Eligibility criteria

Aged 18 years or older. [+5]

a history of intraocular surgery, [+3]

Status: Recruiting

Laser Therapy in the Isotretinoin-Induced Sacroiliitis

The clinical significance of this adverse effect lies in its impact on quality of life and the potential for misdiagnosis. The symptomatology can be severe enough to limit daily activities and may be mistakenly attributed to a primary rheumatic disease, leading to unnecessary long-term immunosuppressive therapy if the temporal link to isotretinoin is not identified. Therefore, a high index of suspicion is crucial for dermatologists, rheumatologists, and primary care physicians alike. Aim: To compare the effectiveness of High-Intensity Laser Therapy (HILT) in reducing pain intensity, in patients diagnosed with Isotretinoin-Induced Sacroiliitis.

Participants needed: 50
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Dec 12, 2025Locations: 1
Eligibility criteria

Aged between 18 and 35 years. [+3]

ankylosing spondylitis or other seronegative spondyloarthritis [+3]

Status: Recruiting

Exercise Therapy for Isotretinoin Users

Isotretinoin (13-cis retinoic acid) is a retinoic acid that is a derivative of vitamin A. Isotretinoin has been used effectively alone in acne treatment for 35 years. However, it has many side effects. Among the musculoskeletal side effects of this treatment, acute sacroileitis is a common condition. In this clinical picture, recovery may last for a few months after discontinuation of isotretinoin treatment. However, it may become permanent in some cases. According to our current knowledge, there is no study in the literature that prescribes exercise therapy for this patient group. This study, planned to investigate the effects of stretching and sacroiliac mobilization exercises on musculoskeletal pain and quality of life, which are among the side effects of isotretinoin treatment.

Participants needed: 160
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

The participant is between the ages of 18-35, [+2]

Presence of any diagnosed rheumatologic disease, [+3]

Status: Recruiting

The Effects of Breathing Exercises and Music Intervention During Labor on Pain Perception, Birth Expectations, and Birth Satisfaction in Primiparous Women

This randomized controlled trial aimed to evaluate the effects of music listening and breathing exercises during labor on pain perception, birth expectations, and birth satisfaction among primiparous women. This randomized controlled trial was conducted in the delivery unit of a hospital located in the Inner Aegean Region of Turkey. The study included 90 primiparous pregnant women admitted for vaginal delivery. Participants without visual, auditory, or neurological impairments were included and randomly assigned into three groups: music intervention group, breathing exercise group, and control group (n=30 in each group). Participants were randomly assigned to one of three groups (Music Intervention, Breathing Exercise, Control) using a computer-generated randomization sequence. Allocation concealment was ensured by using sealed, opaque envelopes prepared by a researcher who was not involved in participant recruitment or assessment. In the music intervention group, participants were introduced to 12 music tracks at 36 weeks of gestation during childbirth preparation classes. Short samples of these tracks were played during the class, and the full tracks were then shared with participants via WhatsApp to encourage regular listening at home. During the prenatal period, participants received regular WhatsApp reminders every few days to listen to the music. During labor, participants were encouraged to listen to music whenever they wished. Additionally, at 4 cm, 6 cm, and 8 cm cervical dilation, all participants in this group listened to their preferred tracks from the playlist for 20 minutes. Pain intensity was measured using the Visual Analog Scale (VAS) before and after each music session. In the breathing exercise group, Lamaze breathing techniques were taught during prenatal classes and practiced throughout the labor process. They were encouraged to practice these exercises throughout labor. At 4, 6, and 8 cm cervical dilation, guided breathing exercises were conducted, and pain was assessed using the Visual Analog Scale (VAS) before and after each exercise. In the control group, participants received routine maternity care. VAS pain assessments were conducted at the same cervical dilation points (4, 6, and 8 cm), without any additional interventions. For all participants, the durations of the first, second, and third stages of labor were recorded and compared across groups. In the postpartum period, the Birth Expectation Scale and Birth Satisfaction Scale were administered. Study data included sociodemographic information, VAS pain scores, and scores from the birth expectation and satisfaction scales.

Participants needed: 90
Trial details
Age: 18-35Biological sex: FemaleType: InterventionalSponsor: Uşak UniversityUpdated: Sep 16, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

The Effect of Emotional Freedom Technique on Psychological Health and Well-being in People With Type 2 Diabetes.

Type 2 diabetes is a major meatbolic condition. People living with Type 2 diabetes come across a wide range of health issues, including psychological health. Specifically, diabetes distress are in high levels among them. Diabetes distress is associated with psychological states such as anxiety, lower levels of self-care, and higher hemoglobin A1c (HbA1c) levels. The Emotional Freedom Technique consists of cognitive and somatic components and is used to heal an individual's negative emotions and manage associated emotional and physical disorders. The basic principle of this technique is to regulate the flow of energy by stimulating the meridian system and to relax the individual while focusing on the emotional reactions that lead to disability. Although the prevalence of psychological problems associated with T2DM and diabetes is increasing, there are not enough studies showing the effect of Emotional Freedom Technique on the psychological well-being of T2DM individuals.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jul 10, 2025Locations: 1
Eligibility criteria

being over 18 years of age, [+3]

be under 18 years of age, [+3]

Status: Recruiting

Evaluation of Aqueous Humor DEL-1 and IL-17 Levels in Diabetic Cataract Patients

By comparing DEL-1 and IL-17 levels in the aqueous humor of diabetic cataract patients with the aqueous humor of non-diabetic patients, we aim to understand the biochemical effects of diabetes-related inflammatory processes in the eye.

Participants needed: 60
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: Uşak UniversityUpdated: Jun 5, 2025Locations: 1
Eligibility criteria

Cataract diagnosed and surgery planned [+2]

Patients with previous intraocular surgery [+4]

Status: Not yet recruiting

Effect of Swimming Exercise on Diastolic Dysfunction

The aim of the study was to determine the rehabilitative effects of 12-week variable intensity swimming exercises on the cardiovascular system in women with diastolic dysfunction. Studies on how variable intensity swimming exercises contribute to the course of the disease in sedentary women with cardiovascular problems are limited. Previous studies generally consisted of studies on the effects of exercise applications on the cardiovascular system in different branches and their effects were determined.

Participants needed: 60
Trial details
Age: 40-60Biological sex: FemaleType: InterventionalSponsor: Uşak UniversityUpdated: Apr 27, 2025Locations: 1
Eligibility criteria

No echocardiographic abnormalities detected except for stage 1 diastolic dysfunc... [+4]

Refusal to sign the informed consent form, [+4]