Clinical trials: Patient-Reported Outcomes
Patient Reported Outcome, Knee Osteoarthritis
Substitution of the PCL in TKA With UC or PS Design
RCT comparing UC and PS TKA
- Conditions
- Patient Reported Outcome, Knee Osteoarthritis, Knee Arthroplasty
- Trial name
- NCT04679857
- Testing
- TKA
- Where
- Germany
- Volunteers
- 127 people
- Sponsor
- Technische Universität Dresden
Physical Activity, Exercise
Physical Activity to Improve Patient Reported Outcomes for Adults With Acute Leukemia
The purpose of this study is to test the efficacy of an evidence-based tailored physical activity program adapted for adults with acute leukemia.
- Conditions
- Physical Activity, Exercise, Acute Leukemia, Consolidation
- Trial name
- Build Stamina (NCT04552912)
- Testing
- Build Stamina Program
- Where
- 2 sites in United States
- Volunteers
- 49 people
- Sponsor
- Duke University
Neurogenic Bladder, Spinal Cord Injuries
Patient Reported Outcomes for Bladder Management Strategies in Spinal Cord Injury
The investigators goal is to create a better understanding of patient reported outcomes for bladder management strategies (clean intermittent catheterization (CIC), indwelling catheter (IDC) and bladder surgery.
- Conditions
- Neurogenic Bladder, Spinal Cord Injuries, Quality of Life, Incontinence
- Trial name
- NBRG-PCORI (NCT02616081)
- Testing
- Clean Intermittent Catheterization, Indwelling Catheter, Surgery
- Where
- 3 sites in United States
- Volunteers
- 1,479 people, healthy volunteers welcome
- Sponsor
- University of Utah
Myopia
Patient Reported Outcomes With WaveLight Plus LASIK
This study is a single-site, single-arm, prospective, observational study of subject satisfaction, quality of vision, and quality of life after bilateral LASIK surgery. Subjects will be assessed 6 months post-operatively.
- Trial name
- NCT07087665
- Testing
- Wavelight Plus
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- OVO LASIK + Lens
Aneurysm Cerebral, AVM
This Three-year Observational Study Involves Patients of All Ages Undergoing Endovascular Treatment for Various Cerebral or Spinal Vascular Conditions. It Aims to Assess Pre- and Post-operative Clinical Conditions, Report Complications, and Identify Preoperative Indicators of Treatment Outcomes. Pat
This three-year observational study involves patients of all ages undergoing endovascular treatment for various cerebral or spinal vascular conditions.
- Conditions
- Aneurysm Cerebral, AVM, DAFV, ESDC
- Trial name
- ONIRIC (NCT06805721)
- Where
- Italy
- Volunteers
- 1,000 people
- Sponsor
- Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Prostate Cancer, Breast Cancer
Remote Monitoring of Patient Reported Outcomes to Improve the Efficacy of the Acute Phase Radiotherapy Review Process
Radiation therapy (RT) is a key component in the treatment of breast and prostate cancer. However, patients may experience significant side effects.
- Trial name
- PROMOTE (NCT06274892)
- Testing
- Remote monitoring PROs
- Where
- Canada
- Volunteers
- 124 people
- Sponsor
- University Health Network, Toronto
Heart Failure
Patient-Reported Outcome Measurement in Heart Failure Clinic
This is a randomized study evaluating the effect of routinely collecting a standardized questionnaire of heart failure health status during heart failure clinic visits.
- Trial name
- PRO-HF (NCT04164004)
- Testing
- Kansas City Cardiomyopathy Questionnaire-12
- Where
- United States
- Volunteers
- 1,249 people
- Sponsor
- Stanford University
Telemedicine, eHealth
Efficacy of the "Consilium" Smartphone App for Detecting Symptoms and Treatment Side Effects in Cancer Patients
The study investigates the influence of the use of a Smartphone App, on changes in general well-being and the occurrence of symptoms during a tumor therapy.
- Trial name
- APP-2 (NCT03578731)
- Testing
- app
- Where
- 18 sites in Austria, Germany and 1 more
- Volunteers
- 224 people
- Sponsor
- OnkoZentrum Zürich AG
Surgical Site Infection, Patient Satisfaction
Effect of Surgical Site Infections on Patient Reported Cosmetic Outcomes in Dermatologic Surgery
This study involves surveying two matched groups of patients that underwent dermatologic surgery at our department. One group had a documented surgical site infection and the other didn't.
- Trial name
- NCT04744961
- Testing
- SCAR-Q survey
- Where
- Sweden
- Volunteers
- 114 people, healthy volunteers welcome
- Sponsor
- Region Skane
Lumbar Disc Herniation
Percutaneous Discectomy to Treat Symptomatic Lumbar Disc Herniation : Evaluation of Clinical Efficiency, Patient Reported Outcomes and Economical Impact by Assessing Time Before Return to Work and Duration of Hospitalization Stay
This study aims to evaluate the clinical (pain) and functional (patient reported outcomes) efficacy of percutaneous discectomies under CT guidance to treat lumbar disc herniations resistant to conservative treatment and nerve…
- Trial name
- NCT05772143
- Testing
- Percutaneous discectomies under CT
- Where
- France
- Volunteers
- 87 people
- Sponsor
- Centre Hospitalier Universitaire de Nice
Patient Reported Outcome Measures, Ovarian Neoplasms
The Possible Influence of Different Follow-up Modalities on Overall Survival in Ovarian Cancer
The study is designed as an observational cohort study, aiming to evaluate, whether a structured recording of symptoms by a mobile app contributes insight in the follow-up modalities of ovarian cancer patients.
- Trial name
- ECOvar (NCT05352217)
- Testing
- Mobile app ovarian cancer followup (ePRO)
- Where
- 4 sites in Switzerland
- Volunteers
- 7 people
- Sponsor
- Stiftung Swiss Tumor Institute
Well-Being, Psychological
Evaluation of Patient-Reported Outcomes Measurement Information System (PROMIS)-29 v2.1 for Postpartum Women
There is no widely used, statistically validated assessment for physical and mental health for the short- to medium-term in a postpartum population.
- Trial name
- NCT06002763
- Testing
- PROMIS-29 v2.1 (Patient-Reported Outcomes Measurement Information System), WHOQoLBREF (World Health Organization Quality of Life Brief Version), EQ-5D-3L1 (not an acronym)
- Where
- Canada
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Stage II Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8, Stage III Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8
Evaluating the Impact of Limited Compared With Intense Post-Operative Surveillance on Patient-Reported Outcomes in Patients With Stage II-III Soft Tissue Sarcoma of the Trunk and Extremities
This phase II trial studies how anxiety is affected by 2 types of follow-up after surgery, limited follow-up and intense follow-up, in patients with stage II-III soft tissue sarcoma of the trunk and extremities.
- Conditions
- Stage II Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8, Stage III Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8, Stage IIIA Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8, Stage IIIB Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8
- Trial name
- NCT04751409
- Testing
- Chest Radiography, Computed Tomography, Follow-Up
- Where
- United States
- Volunteers
- 227 people
- Sponsor
- M.D. Anderson Cancer Center
Radiotherapy
Comparison Between Virtual vs in Person on Treatment Follow-up Visits of Radiotherapy
This study aims to evaluate the logistical feasibility and implementation of virtual versus in-person on-treatment follow up visits in a high-volume radiation oncology setting.
- Trial name
- NCT07724548
- Where
- Pakistan
- Volunteers
- 180 people
- Sponsor
- Shaukat Khanum Memorial Cancer Hospital & Research Centre
Diabetes Mellitus, Type 1
Insulin Delivery Using the DBLG1 Closed-loop on Glycemic Control and PROMs in Adults Living With Type 1 Diabetes
To evaluate the impact of the DBLG1 hybrid closed-loop system on glycemic control and patient-reported outcomes in adults living with type 1 diabetes under real-life conditions.
- Trial name
- INLOOP (NCT06154135)
- Where
- 12 sites in Belgium
- Volunteers
- 165 people
- Sponsor
- Erasme University Hospital
Incontinence, Neurogenic Bladder Dysfunction
RElax & feeL at EASE (RELEASE)
This multicenter, parallel-group, randomized controlled trial (RELEASE) aims to evaluate the efficacy of two educational approaches on acceptance and adherence to intermittent catheterization (IC) among adult male patients.
- Conditions
- Incontinence, Neurogenic Bladder Dysfunction, Urinary Retention
- Trial name
- RELEASE (NCT07084376)
- Testing
- Enhanced Educational Program for Intermittent Catheterization, Standard Education Group
- Volunteers
- 64 people
- Sponsor
- Stefania Musco
Temporomandibular Disorders (TMD), Wilkes 1 and 2
Art-Based Pain Assessment Tool in Patients With Temporomandibular Joint Disorders
Title of Study: Assessment of the Impact of Art-Based Pain Assessment Tool on Pain Communication, Joint Function, and Anxiety in Patients with Temporomandibular Disorders (TMD): A Randomized Controlled Trial Location: King…
- Conditions
- Temporomandibular Disorders (TMD), Wilkes 1 and 2, TMJ Pain, TMJ - Oral &Amp;Maxillofacial Surgery
- Trial name
- NCT07018791
- Testing
- Standard TMD Assessment, Artistic Pain Exploration (APE) Method
- Where
- Saudi Arabia
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- King Abdulaziz University
Chronic Obstructive Pulmonary Disease (13645005)
Advancing the Patient Experience in Chronic Obstructive Pulmonary Disease (APEX COPD)
APEX COPD is registry to provide a mechanism to standardize, store and utilize data to enable greater power to answer key research questions, and to improve patient outcomes in COPD primary care.
- Trial name
- APEX COPD (NCT04285047)
- Testing
- Advancing Patient Experience (APEX) in COPD
- Where
- 4 sites in United States
- Volunteers
- 4,500 people
- Sponsor
- Optimum Patient Care
Edentulous Alveolar Ridge
The Impact of the Adequacy of Keratinized Mucosa on Peri-implant Tissue Health and Patient-reported Outcomes
This study aims to conduct a cross-sectional study to compare the differences in clinical indices, patient-reported outcomes, and levels of inflammatory factors in peri-implant gingival crevicular fluid between sites with…
- Trial name
- NCT07124416
- Testing
- No intervention
- Where
- China
- Volunteers
- 150 people
- Sponsor
- The Dental Hospital of Zhejiang University School of Medicine
Leukemia, Lymphoma
Leukemia and Lymphoma Society (LLS) Services Impact on Outcomes and Care
The purpose of this study is to learn about the impact that the services and programs provided by Blood Cancer United (formerly, The Leukemia and Lymphoma Society) have among patients with blood cancer, such as access to care…
- Conditions
- Leukemia, Lymphoma, Myeloma, Myelodysplastic Syndromes
- Trial name
- NCT05745285
- Testing
- LLS Program
- Where
- 3 sites in United States
- Volunteers
- 400 people
- Sponsor
- University of Miami
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