Clinical trials: Self Report
ADHD Specifically With Executive Function Impairment
Safety and Efficacy of SPD489 on Executive Function Behaviors in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
The primary objective of the study is to evaluate the efficacy of SPD489 compared to placebo on executive function (self-regulation) behaviors in adults with ADHD who report clinically significant impairment of executive function…
- Trial name
- NCT01101022
- Testing
- SPD489
- Where
- 39 sites in United States
- Volunteers
- 161 people
- Sponsor
- Shire
Abdominal Pain
Study to Evaluate the Efficacy and Safety of Hyoscine Butylbromide Tablets for the Treatment of Occasional or Recurrent Episodes of Gastric or Intestinal Spasm-like Pain or Discomfort
In contrast with Hyoscine Butylbromide Capsule 10mg, Study is to evaluate the efficacy and safety of Hyoscine Butylbromide tablets 10 mg (20mg, 3 times daily, orally) over a period of 3 days for the treatment of occasional or…
- Trial name
- NCT02242305
- Testing
- Hyoscine Butylbromide - Tablet, Hyoscine Butylbromide - Capsule
- Volunteers
- 302 people
- Sponsor
- Boehringer Ingelheim
Vaginal Infection, Vaginal Discharge
Evaluation of a Postcoital Sponge on Self-Reported Vaginal Health Parameters
LiviWell has developed a product designed for postcoital semen absorption. Previous studies have demonstrated the product rapidly absorbs semen, and leads to less symptoms of postcoital vaginal microbiome disruption such as…
- Conditions
- Vaginal Infection, Vaginal Discharge, Vaginosis, Sexual Dysfunction
- Trial name
- NCT06530186
- Testing
- LiviWell Postcoital Vaginal Insert
- Where
- United States
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Atlantic Health System
Pregnancy Related, Oral Health
Self Reported Oral Health, Awareness and Attitude Towards Dental Care Among Pregnant Women
Purpose/Objective of the study: The main objective of the study is to investigate oral health awareness and attitudes towards oral health among Norwegian pregnant women and assess the impact of information about oral hygiene on…
- Conditions
- Pregnancy Related, Oral Health, Attitude, Oxidative Stress
- Trial name
- NCT01675180
- Testing
- Information, Control
- Where
- Norway
- Volunteers
- 97 people, healthy volunteers welcome
- Sponsor
- University of Tromso
Self Reported Ratings of Hunger
The Effects of Processed Whole Orange on Subjective Ratings of Satiety
The study is a human dietary test meal study that is a randomized, controlled, double blind, cross over design with 3 intervention arms that will investigate the subjective ratings of satiety in response to different levels of…
- Trial name
- POAS (NCT02116023)
- Testing
- Orange flavored beverage
- Where
- United Kingdom
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- PepsiCo Global R&D
Endometriosis, Pelvic Pain
Machine Learning for Early Diagnosis of Endometriosis(MLEndo)
The project aims to create a large prospective data bank using the Lucy medical mobile application and collect and analyze patient profiles and structured clinical data with artificial intelligence.
- Conditions
- Endometriosis, Pelvic Pain, Infertility, Female
- Trial name
- MLEndo (NCT06147687)
- Testing
- Self reported data collection
- Where
- 2 sites in Hungary
- Volunteers
- 10,000 people, healthy volunteers welcome
- Sponsor
- Semmelweis University
Sleep Disturbance, Poor Sleep Quality
A Trial to Examine the Efficacy of a Supplement Gummy to Improve Sleep Quality and Quantity
This single-group trial evaluates the efficacy of FlavCity's Sleep Gummy supplement on sleep health in adults aged 20-50 who self-report issues with sleep.
- Conditions
- Sleep Disturbance, Poor Sleep Quality, Insomnia (Self-reported, Non-diagnosed)
- Trial name
- NCT07781332
- Testing
- Sleep Gummy Intervention
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- DTBE, LLC dba FlavCity
Cancer
eRAPID Feasibility Pilot Study in Pelvic Radiotherapy
The purpose of the Electronic Patient Self-Reporting of Adverse-events: Patient Information and aDvice (eRAPID) programme is to determine whether eRAPID (an online system for patients to self-report symptoms and side effects) can…
- Trial name
- eRAPID-RT (NCT02747264)
- Testing
- eRAPID
- Where
- 2 sites in United Kingdom
- Volunteers
- 167 people
- Sponsor
- University of Leeds
Colorectal Cancer Control and Prevention
Self-Reported Colorectal Cancer Screening Uptake
This randomized controlled trial evaluated the effect of a Health Belief Model-based multicomponent education program on colorectal cancer screening completion, knowledge, health beliefs, and screening attitudes among adults aged…
- Trial name
- CRC-HBM (NCT07778875)
- Testing
- Health Belief Model-Based Colorectal Cancer Education Program
- Where
- Turkey (Türkiye)
- Volunteers
- 176 people, healthy volunteers welcome
- Sponsor
- Bartın Unıversity
Anxiety
A Study Comparing Immediate Treatment to Deferred Treatment With the Fisher Wallace (FW) Stimulator FW-200 Device for the Treatment of Self-reported Anxiety in First Responders
The goal of this clinical trial is to learn if the Fisher Wallace Stimulator FW-200 experimental device is effective at treating self-reported anxiety in first responders.
- Trial name
- NCT07093736
- Testing
- FW-200
- Where
- 2 sites in United States
- Volunteers
- 220 people
- Sponsor
- Fisher Wallace Laboratories
Insomnia (Self-reported, Non-diagnosed), Hypertension
Acupressure to Improve Insomnia Among the Elderly With Hypertension
The goal of this study is to evaluate the feasibility and the effect of self-acupressure on improving insomnia among the elderly with hypertension who reported insomnia (using the Insomnia Severity Index questionnaire) The main…
- Conditions
- Insomnia (Self-reported, Non-diagnosed), Hypertension, Elder
- Trial name
- NCT07827560
- Testing
- Acupressure to improve insomnia
- Where
- Vietnam
- Volunteers
- 94 people
- Sponsor
- Phenikaa University
Ankle Injuries, Ankle Inversion Sprain
External Versus Internal Feedback in Patients With Chronic Ankle Instability
Although altered biomechanics has been well documented as an impairment associated with chronic ankle instability (CAI), effective interventions targeting biomechanics with long-term outcomes measuring patient-reported outcomes…
- Trial name
- NCT04131842
- Testing
- External focus of attention visual feedback, External focus of attention auditory feedback, Internal focus of attention video feedback
- Where
- United States
- Volunteers
- 48 people
- Sponsor
- University of North Carolina, Charlotte
Depression, Anxiety
Mental Health Promotion Interventions Among Migrant Workers in China
The goals of this research were to conduct a mental health intervention study for reducing self-reported depression and anxiety among migrant workers in a labor-intensive industry in China and to assess the effectiveness of the…
- Trial name
- NCT02009358
- Testing
- mental health promotion
- Volunteers
- 913 people
- Sponsor
- Peking University
Joint Pain
Short-term Impact of Cyplexinol® on Self-reported Joint Pain
In this study, the impact of 900 mg Cyplexinol® taken daily on joint pain over a period of 15 days in comparison with a placebo will be determined using a cross-over double blind design with a 13 day wash out period.
- Trial name
- NCT04764110
- Testing
- Cyplexinol
- Where
- United States
- Volunteers
- 18 people
- Sponsor
- University of Memphis
Perimenopause
Radicle Revive™ CSP: A Trial Evaluating Plant-Based Health and Wellness Products on Perimenopausal Women's Self-Reported Health Issues and Outcomes
A randomized, double-blind, placebo-controlled, trial evaluating plant-based health and wellness products on perimenopausal women's self-reported health issues and outcomes
- Trial name
- NCT07148011
- Testing
- Revive Product Form - Active
- Where
- United States
- Volunteers
- 900 people, healthy volunteers welcome
- Sponsor
- Radicle Science
Pain
The Efficacy of Pain Management With Self-reporting Pain Monitoring System in Cancer Patient
To compare the pain scales between clinician evaluated and reported with wearable device by patients.
- Trial name
- pain (NCT03117075)
- Testing
- using device for scoring pain scale, named "ANAPA®"
- Where
- 2 sites in South Korea
- Volunteers
- 68 people
- Sponsor
- DERSHENG SUN
Quality of Life
Impact of Different Carbohydrate Feedings on a Hydrogen Breath Curve and Self-reported Gastrointestinal Complaints
GI distress is widely prevalent among athletes, ranging from 30 to 90% in recreationally and professionally active athletes. As the recipient of nutrients, the gastrointestinal (GI) tract plays an important role in athleticism.
- Trial name
- NCT06648967
- Testing
- Supplementation with a multi-ingredient whey supplement
- Where
- United States
- Volunteers
- 8 people, healthy volunteers welcome
- Sponsor
- Arizona State University
Physical Activity
Characterisation of Objectively Measured Physical Activity and Self-reported Habitual Exercise
This study aims to observe participants' physical activity (PA) using a blinded multisensor physical activity monitor as they go about their typical daily physical activities across a 6-week time frame.
- Trial name
- NCT05250700
- Where
- United Kingdom
- Volunteers
- 66 people, healthy volunteers welcome
- Sponsor
- University of Bath
Periodontitis, Diagnosis
Self-detection and Professional Screening Strategies for Early Detection of Periodontal Disease
The majority of the burden of periodontal diseases in the population remain undetected. Self-detection and confirmation with simple, non-clinical tests may improve early case detection and access to the needed level of care.
- Conditions
- Periodontitis, Diagnosis, Self-Assessment
- Trial name
- NCT05513599
- Where
- China
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Anatomic Stage 0 Breast Cancer AJCC v8, Anatomic Stage I Breast Cancer AJCC v8
Web-Based Symptom Monitoring and Self-Management Portal (YES) for Adolescent and Young Adult Breast Cancer Survivors
This clinical trial compares a web-based patient-reported symptom monitoring and self management portal, the Young, Empowered \& Strong (YES), to standard therapy in managing symptoms in adolescent and young adult breast cancer…
- Conditions
- Anatomic Stage 0 Breast Cancer AJCC v8, Anatomic Stage I Breast Cancer AJCC v8, Anatomic Stage IA Breast Cancer AJCC v8, Anatomic Stage IB Breast Cancer AJCC v8
- Trial name
- YES (NCT04906200)
- Testing
- Best Practice, Internet-Based Intervention, Survey Administration
- Where
- 3 sites in United States
- Volunteers
- 400 people
- Sponsor
- Ohio State University Comprehensive Cancer Center