Assessment, Self

6

Review clinical trials related to Assessment, Self. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluation Criteria, Diagnostic Criteria, Surgical Indications, and Establishment of Surgical Standards for "Cerebral Tinnitus Syndrome" Caused by Internal Jugular Vein Stenosis.

"Cerebral Tinnitus," also known as "cranial tinnitus," refers to the patient-reported perception of intracranial sounds. It often presents as "Cerebral Tinnitus Syndrome," which includes symptoms such as tinnitus with hearing loss, headaches, a heavy head sensation, blurred vision, neck and shoulder discomfort, sleep disturbances, anxiety, and depression. Due to limited awareness of cerebral tinnitus, patients frequently seek treatment across multiple facilities without success, severely impacting their and their families' lives and work. Xunming Ji and colleagues have pointed out that cerebral tinnitus results from stenosis of the cerebral or internal jugular veins (IJVS), which impairs cerebral venous outflow and the clearance of metabolic "waste," leading to chronic metabolic damage to brain cells. Currently, studies on the diagnosis and treatment of IJVS-induced cerebral tinnitus, both domestically and internationally, are primarily case reports, lacking systematic evaluation, diagnostic, and treatment standards, which significantly impacts patient outcomes. Our project team is the first to establish evaluation criteria, diagnostic standards, surgical indications, and surgical standards for "Cerebral Tinnitus Syndrome." In preliminary work, we performed internal jugular vein (IJV) decompression on 32 cerebral tinnitus patients, resulting in an IJV morphological improvement rate of 84.3%, a blood flow improvement rate of 75.0%, and a cerebral tinnitus syndrome improvement rate of 62.5%. To date, we have completed 88 IJV decompression surgeries, making ours the largest clinical center for such cases worldwide. We continue to refine these standards, notably introducing new intraoperative standards for IJV "release" and "high perfusion,". To validate and further study these standards, this project plans to perform IJV decompression surgery on 107 cerebral tinnitus patients affected by IJVS. We aim to establish a cerebral tinnitus database and develop a cerebral tinnitus evaluation scale to standardize evaluation criteria, diagnostic standards, surgical indications, and surgical standards, ultimately advancing clinical diagnosis and treatment of Cerebral Tinnitus Syndrome

Participants needed: 369
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Beijing Shijitan Hospital, Capital Medical UniversityUpdated: May 1, 2026Locations: 1
Eligibility criteria

Age between 18 and 75 years, with no gender restriction. [+4]

Patients with a history of cranial surgery or diagnosed intracranial space-occup... [+4]

Status: Recruiting

Isometric Strength and Joint Mobility Profile in Elite Artistic Swimmers Across Competitive Categories

This cross-sectional observational study aims to establish reference values for joint mobility and isometric muscle strength in elite artistic swimmers across different competitive categories. The study will analyze inter-limb asymmetries and agonist-antagonist strength ratios in upper and lower limbs. Additionally, relationships between isometric strength, countermovement jump performance, and handgrip strength will be explored to assess their utility as functional performance indicators. Participants will be assessed during national team training camps using standardized, validated measurement protocols. The findings are expected to contribute to the identification of sport-specific functional profiles and potential injury risk factors in artistic swimming.

Participants needed: 45
Trial details
Age: 14-50Biological sex: AllType: ObservationalSponsor: University of VigoUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

Elite artistic swimmers selected for the Spanish National Artistic Swimming Team... [+3]

Acute musculoskeletal or joint injury affecting the tested regions (shoulder, hi... [+2]

Status: Recruiting

Reliability of PHAS in Postural Hyperkyphosis

This observational, cross-sectional study aims to evaluate the reliability of the Postural Habits and Awareness Scale (PHAS) in patients with postural hyperkyphosis. The PHAS is designed to assess individuals' postural awareness and habits through four subscales. A total of 128 participants diagnosed with postural hyperkyphosis will complete the PHAS and the Kyphosis-Specific Spinal Appearance Questionnaire (KSSA). Test-retest reliability will be assessed by reapplying the PHAS after two weeks. Internal consistency, test-retest reliability, and concurrent validity will be analyzed. The study aims to provide a valid and reliable tool for evaluating postural awareness in clinical practice and future rehabilitation studies.

Participants needed: 128
Trial details
Age: 8-65Biological sex: AllType: ObservationalSponsor: Istanbul University - CerrahpasaUpdated: Oct 1, 2025Locations: 1
Eligibility criteria

Age between 8 and 65 years [+3]

Presence of scoliosis or other spinal deformities [+5]

Status: Recruiting

The Mere-measurement Effect of Patient-reported Outcomes

The use of patient-reported outcome (PROs) have become increasingly commonplace across many healthcare settings over the past two decades. The value of PROs is now acknowledged by healthcare providers and patients alike. However, to date, little is known about the best practices for formulating PRO measures (PROMS), but even more specifically, the effect had on the responding patients as a result of item word choice, emotional valence, or frequency of use. That is, 1) does the positive or negative wording of items affect the patient's perspective on the latent variable, 2) is there a degree of subliminal influence or measurement effects on their behaviour resulting from exposure to PROs, and finally, 3) is such an effect amplified with repeated exposure?

Participants needed: 170
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medical University of ViennaUpdated: May 14, 2025Locations: 1
Eligibility criteria

Strong English skills* [+6]

Under the age of 18

Status: Not yet recruiting

Multidirectional Isometric Assessment of the Hip

With the exception of the shoulder, the hip is among the most frequently injured areas in swimmers. Despite this, hip injuries are often overlooked in training and prevention programmes. Such neglect can cause significant damage to muscles, particularly the adductors, and the joint itself, potentially requiring arthroscopic surgery or even leading to secondary injuries in related structures such as the knee. Furthermore, hip strength and range of motion directly affect swimmers' underwater kicking speed. Although hip assessments are common in other sports, like football, for injury prevention and performance analysis-both dynamically and isometrically-isometric testing is particularly recommended due to its higher reproducibility. Therefore, this study aims to validate a multidirectional isometric hip test in swimmers and examine agonist-antagonist muscle ratios in young advanced swimmers. A comparative analysis will be conducted on 30 elite swimmers. This will include a descriptive analysis of the group and comparative analyses between breaststroke/non-breaststroke swimmers and between genders. Maximum isometric contractions of both lower limbs will be measured using a Chronojump force sensor (Boscosystem, Barcelona, Spain). Athletes will stand on a step positioned centrally within a rack or cage, either laterally or frontally depending on the movement assessed (ABD-ADD or flexion-extension, respectively). They will grip the appropriate supports with their hands and perform three maximal efforts of each movement lasting 3 seconds, without compensatory actions (any attempt with compensations will be discounted). There will be a 20-second rest between attempts. All three attempts will be recorded. To assess measurement reliability, tests will be repeated after 48 hours for subsequent comparison.

Participants needed: 55
Trial details
Age: 14-18Biological sex: AllType: InterventionalSponsor: University of VigoUpdated: Apr 27, 2025
Eligibility criteria

Aged between 14 and 18 years. [+2]

Swimmers with any current hip or lower limb pathology. [+4]

Status: Not yet recruiting

Reliability of the Gyko Inertial Sensor System in Evaluating Jumping and Postural Stability Parameters in Healthy Adults

The aim of the study is to examine the Gyko inertial sensor system in healthy adults. In the study, jump and postural control parameters are assessed with a one-week interval. To evaluate intra-rater reliability, ICC, SEM, and MDC values will be calculated.

Participants needed: 55
Trial details
Age: 18-35Biological sex: AllType: ObservationalSponsor: Hacettepe UniversityUpdated: Nov 6, 2024
Eligibility criteria

being between the ages of 18 and 35 [+2]

Having known neurological, rheumatological, or musculoskeletal system problems.