Clinical trials: Self-report Questionnaire
Psychological Distress
Psychological Distress in Emerging Adulthood: A Longitudinal Study
Emerging adulthood (18-29 years) is a critical stage in lifespan development. During this stage, people experience instability: shifts from their families of origin, breakups of relationships and job changes are frequent before…
- Trial name
- DistressEA (NCT04596345)
- Where
- Ecuador
- Volunteers
- 1,168 people, healthy volunteers welcome
- Sponsor
- Universidad de las Americas - Quito
Physiologic Monitoring, Self-report Questionnaire
Can the Belgian Coastal Environment Improve Physical and Cognitive Health in Older Adults?
The goal of this interventional study is to learn if exposure to coastal environments improves the physical and cognitive health of older adults over the age of 60.
- Conditions
- Physiologic Monitoring, Self-report Questionnaire, Sleep Quality, Cognitive Function
- Trial name
- NCT06893224
- Testing
- Coastal exposure, Urban exposure
- Where
- Belgium
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- University Ghent
Delivery of Health Care, Genetic Testing
Supporting Just-In-Time Consent for Prenatal Screening: The INFORM Study
This clinical trial is about prenatal genetic screening. It will test an intervention to help people make decisions about screening. The intervention is a short set of information cards about screening.
- Conditions
- Delivery of Health Care, Genetic Testing, Humans, Pregnancy
- Trial name
- NCT07557303
- Testing
- Mobile-based Educational Intervention
- Where
- 3 sites in United States
- Volunteers
- 1,400 people, healthy volunteers welcome
- Sponsor
- Case Western Reserve University
Rheumatoid Arthritis
Evaluating Kineret® (Anakinra) in Rheumatoid Arthritis (RA) Subjects Using aSelf-Reported Questionnaire
The primary purpose of this study is to assess the ease-of-use of SimpleJectTM compared to pre-filled syringe(s) when using Kineret® in RA subjects.
- Trial name
- NCT00121043
- Testing
- SimpleJectTM, Kineret® (Anakinra)
- Sponsor
- Amgen
Lupus Erythematosus, Systemic
Validation of Patient E-tool to Measure Systemic Lupus Activity
Validation of a self-questionnaire (SLEDAI-P/LUPIN) completed by the patient to measure the activity of the systemic lupus, in order to improve the patient's empowerment.
- Trial name
- OPTIMISE (NCT05763225)
- Where
- 31 sites in France, Guadeloupe and 1 more
- Volunteers
- 450 people
- Sponsor
- Association Francaise du Lupus et Autres Maladies Auto-immunes (AFL+)
Smartphone Addiction, Game Addiction, Video
Exploring the Effects of Smartphone and Game Addiction on Activity, Sleep, Stress, and Pain in Youth
This study aims to examine the relationship between smartphone and digital game addiction and various health indicators, including physical activity level, sleep quality, stress, fatigue, and musculoskeletal pain among young…
- Conditions
- Smartphone Addiction, Game Addiction, Video, Musculoskeletal Pain Disorder, Sleep
- Trial name
- NCT06994104
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 194 people, healthy volunteers welcome
- Sponsor
- Istanbul University - Cerrahpasa
Chronic Kidney Disease Stage 5, Dialysis
An Evaluation of the KCCQ Score in Predicting Cardiovascular Risk in Dialysis Patients
Cardiovascular Disease (CVD) is the main complication and the most important cause of death in CKD patients. As the disease progresses, the incidence of cardiovascular disease in CKD patients gradually increases, especially in…
- Conditions
- Chronic Kidney Disease Stage 5, Dialysis, Heart Failure
- Trial name
- NCT06542016
- Where
- China
- Volunteers
- 136 people
- Sponsor
- Shenzhen Second People's Hospital
ACL Tear, ACL - Anterior Cruciate Ligament Deficiency
Proprioceptive Isokinetic Repositioning, Functional Testing, and a Self-reported Questionnaire Before and After Anterior Cruciate Ligament Reconstruction
This prospectively study aims to evaluate the evolution of knee joint proprioception on isokinetic dynamometer before and after Anterior Cruciate Ligament (ACL) reconstruction and its relationships with muscle strength, self…
- Trial name
- PRO-ACL (NCT04058574)
- Testing
- Proprioception measurement on isokinetic dynamometer
- Where
- 2 sites in France
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- University Hospital, Caen
Periodontal Disease, Gingivitis
Diagnostic Accuracy of Oral Images, OPGs, Biomarkers and Questionnaires vs. Clinical Assessment for Periodontal Disease (PostNCT07164573)
This multi-center, cross-sectional diagnostic trial evaluates the accuracy of multiple non-invasive screening tools-including self-reported questionnaires, intra-oral photographs, orthopantomographs (OPGs), intraoral scans (IOS)…
- Conditions
- Periodontal Disease, Gingivitis, Periodontitis
- Trial name
- NCT07406867
- Where
- 3 sites in China, Italy and 1 more
- Volunteers
- 2,000 people, healthy volunteers welcome
- Sponsor
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Periodontal Diseases, Gingivitis
Diagnostic Accuracy of Oral Images, OPGs, and Questionnaires vs. Clinical Assessment for Periodontal Disease
This is a multi-center, cross-sectional diagnostic study aimed at evaluating the accuracy of various non-invasive methods-including self-reported questionnaires, intra-oral photographs, smartphone images, intraoral scans (IOS)…
- Conditions
- Periodontal Diseases, Gingivitis, Periodontitis
- Trial name
- NCT07164573
- Where
- China
- Volunteers
- 2,000 people, healthy volunteers welcome
- Sponsor
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Ankle Injuries, Instability, Joint
Turkish Language and Cross-cultural Adaptation of the Cumberland Ankle Instability Tool
Cumberland Ankle Instability Tool (CAIT) is a valid patient-reported outcome measure (PROM) to determine the presence of ankle instability (AI) and assess its severity.
- Trial name
- CAIT-TR (NCT05977660)
- Testing
- Cumberland ankle instability tool for diagnose to determine ankle instability and its severity
- Where
- Turkey (Türkiye)
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- Eskisehir Technical University
Post-COVID-19 Related Fatigue
Disease-related Fatigue Monitoring Based on Body Signals Measured on the Skin
This study investigates the use of physiological parameters as predictors of disease-related fatigue. For that purpose, wearable devices are used to monitor post-COVID-19 patients during their stay in a rehabilitation clinic.
- Trial name
- Fatignals (NCT05853055)
- Testing
- Respiratory training
- Where
- Switzerland
- Volunteers
- 33 people
- Sponsor
- Simon Annaheim
Perioperative, Children
Pediatric Perioperative Satisfaction Questionnaire
The aim of this study is to develop and validate a self-report questionnaire to evalutate the satisfaction of the children after surgery.
- Conditions
- Perioperative, Children, Satisfaction
- Trial name
- NCT04608968
- Where
- 6 sites in France
- Volunteers
- 600 people, healthy volunteers welcome
- Sponsor
- University Hospital, Montpellier
Breast Cancer
The Distress-barometer: Face-to-face Interviews or Written Self-report Questionnaires?
Breast cancer is the most prevalent cancer among women worldwide [1]. 5 years after diagnosis, up to 87% survives. A substantial group of these survivors report reduced physical, psycho social and cognitive functioning.
- Trial name
- NCT03357744
- Testing
- distress barometer
- Volunteers
- 59 people
- Sponsor
- KU Leuven
Gastrointestinal Disorders, Functional
Web-based Management of Pediatric Functional Abdominal Pain
Functional abdominal pain (FAP), a pediatric pain condition without significant organic pathology, is a precursor to chronic pain and high healthcare utilization in young adulthood.
- Trial name
- NCT02327377
- Testing
- Online Cognitive Behavior Therapy, Online Education
- Where
- United States
- Volunteers
- 344 people
- Sponsor
- Vanderbilt University Medical Center
Periodontitis and Treatment Need
Evaluation of a New Self-reported Tool for Periodontitis Screening
200 patients took part in the questionnaire and were examined using the PSI. Thereafter the participants were divided into two groups, non-periodontitis persons (group 1; PSI 0-2) and periodontitis persons (group 2; PSI 3-4).
- Trial name
- NCT02754401
- Testing
- 16 Items, PSI
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Renatus, Antonio Renatus, Dent., M.Sc
Mild Intellectual Disability, Borderline Intellectual Functioning
Improving the Cognitive Accessibility of Self-reports for People With ID
In the proposed study, the investigators aim to investigate whether the existing ABAS-3 self-report questionnaire is suitable to be completed meaningfully by individuals who are perceived as having mild intellectual disability…
- Trial name
- NCT05857592
- Testing
- Adaptive functioning self-report questionnaire, Adaptive functioning self-report questionnaire - adapted
- Where
- Netherlands
- Volunteers
- 20 people
- Sponsor
- Koraal
Shoulder Pain
The Chinese Version of the American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form Questionnaire, Patient Self-report Section: A Cross-cultural Adaptation and Validation Study
Background: The patient self-report section of the American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form (ASESp) is one of the most validated and reliable assessment tools.
- Trial name
- NCT04755049
- Testing
- The Chinese version of the American Shoulder and Elbow Surgeons standardized shoulder assessment form questionnaire
- Where
- Taiwan
- Volunteers
- 120 people
- Sponsor
- National Cheng-Kung University Hospital
Spinal Cord Injuries
Development and Validation of a Bowel-routine-based Self Report Questionnaire for Sacral Sparing After Spinal Cord Injury
To develop a self-administered tool for assessment of sacral sparing after spinal cord injury (SCI) and to test its validity in individuals with SCI.
- Trial name
- NCT04951297
- Testing
- None, just observation
- Volunteers
- 102 people
- Sponsor
- Peking University Third Hospital
Multiple Sclerosis
Assessing Relapse in Multiple Sclerosis (ARMS) Questionnaire
This Phase 4 pilot cross-sectional descriptive/exploratory study is to be conducted in clinical practice settings (including MS (Multiple sclerosis) specialty clinics, general neurology practices, or other academic or private…
- Trial name
- ARMS (NCT01547351)
- Testing
- ARMS Questionnaire
- Where
- 5 sites in United States
- Volunteers
- 103 people
- Sponsor
- Mallinckrodt