Clinical trials: Patient-reported Outcome
Preoperative Anxiety, Orthopedic Surgery
Preoperative Anxiety and One-year Patient-reported Outcomes in Orthopedic Surgery Patients Receiving Enhanced Recovery After Surgery or Conventional Care
This study investigates whether an Enhanced Recovery After Surgery (ERAS) program can help orthopedic surgery patients feel less anxious before their operation and recover better one year after surgery, compared to conventional…
- Conditions
- Preoperative Anxiety, Orthopedic Surgery, Patient Reported Outcome (PRO)
- Trial name
- ERAS-APO (NCT07706244)
- Testing
- Enhanced Recovery After Surgery (ERAS) pathway, Conventional care group
- Where
- Taiwan
- Volunteers
- 220 people
- Sponsor
- Buddhist Tzu Chi General Hospital
Patient-Reported Outcome Measures (PROMs), Pragmatic Trial
A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study
The goal of this pragmatic clinical trial is to learn if the WE BEAT program, a 5-week group-based online wellbeing and skill-building program, can help teens with congenital heart disease (CHD) improve their ability to handle…
- Conditions
- Patient-Reported Outcome Measures (PROMs), Pragmatic Trial, Adolescent Congenital Heart Disease, Resiliency-building Intervention
- Trial name
- PHN WBC (NCT07525843)
- Testing
- Telemedicine-based resiliency-building intervention
- Where
- 14 sites in United States
- Volunteers
- 390 people
- Sponsor
- Carelon Research
Dental Implant, Implant Therapy
Do Immediate Digital Workflows Increase Patient Value?
This two-center randomized controlled trial will evaluate whether an immediate digital posterior implant workflow provides greater patient-defined value than a delayed digital workflow in adults requiring single posterior implant…
- Conditions
- Dental Implant, Implant Therapy, Immediate Dental Implant Placement, Delayed Implant
- Trial name
- ITI PROM RCT (NCT07656597)
- Testing
- Immediate digital posterior implant workflow, Delayed digital posterior implant workflow
- Where
- 2 sites in Germany, Hong Kong
- Volunteers
- 50 people
- Sponsor
- Heinrich-Heine University, Duesseldorf
Abdominal Pain, Gallstone; Colic
RELIEF-pathway in Patients With Upper Abdominal Pain
Upper abdominal pain (UAP) is a common symptom and frequently the reason to visit the hospital. The prevalence of epigastric pain in the Dutch population is estimated to be as high as 37%.
- Conditions
- Abdominal Pain, Gallstone; Colic, Dyspepsia, Irritable Bowel Syndrome
- Trial name
- RELIEF (NCT06002516)
- Testing
- RELIEF-pathway
- Where
- Netherlands
- Volunteers
- 471 people
- Sponsor
- Radboud University Medical Center
Lung Neoplasms, Non-Small Cell Lung Cancer, Postoperative Complications
Smartphone-based Remote Symptom Monitoring to Improve Postoperative Rehabilitation Exercise Adherence After Video-assisted Thoracic Surgery (VATS) for Lung Cancer
Brief Summary: This randomized controlled trial aims to evaluate whether active remote symptom monitoring and management via a smartphone app utilizing electronic patient-reported outcomes (ePRO) can improve adherence to…
- Conditions
- Lung Neoplasms, Non-Small Cell Lung Cancer, Postoperative Complications, Patient Reported Outcome Measures, Telerehabilitation
- Trial name
- NCT05990946
- Testing
- ePRO based Remote Symptom Management provide by a mobile phone app
- Where
- China
- Volunteers
- 736 people
- Sponsor
- Zhongshan People's Hospital, Guangdong, China
Breast Cancer, Patient Reported Outcomes
Breast Cancer Patient Engagement With Patient Reported Outcome Measure Survey
The purpose of this research protocol is to measure Patient Reported Outcome Measures (PROMs) in breast cancer patients. PROM results will be provided to patients and providers and the investigators will evaluate the relationship…
- Trial name
- NCT03995082
- Testing
- Patient Reported Outcome Measure Survey result feedback
- Where
- 3 sites in United States
- Volunteers
- 925 people
- Sponsor
- University of Colorado, Denver
Stroke, Osteopathic Medicine
Examining Relationships Between Musculoskeletal Function Measurements of Movement Efficiency and Nervous System Function After Chronic Stroke
Stroke remains the leading cause of severe disability, and survivors frequently have incomplete recovery. More than half of older survivors have impaired mobility which contributes to poorer quality-of-life (QoL) and suffering.
- Conditions
- Stroke, Osteopathic Medicine, Physical Examination, Heart Rate Variability (HRV)
- Trial name
- SOMADC-CC (NCT07737873)
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- University of California, Davis
Haemodiafiltration, Haemodialysis
Adequacy of Haemodiafiltration: Middle Molecules Clearance, Patients Reported Outcomes and Sodium Balance
The goal of this observational study is to understand the differences in terms of middle molecules clearance and patient outcomes in High (>23Litres (L)) vs Low (<23 L) convection volume (CV) Hemodiafiltration (HDF) and to…
- Conditions
- Haemodiafiltration, Haemodialysis, Patient Reported Outcome Measurements, Nutrition
- Trial name
- NCT07717255
- Where
- United Kingdom
- Volunteers
- 300 people
- Sponsor
- East and North Hertfordshire NHS Trust
Patient Reported Outcomes, Patient Satisfaction
Patient-reported Outcome and Patient-reported Experience After Status Epilepticus
Status epilepticus (SE) is a common life-threatening neurological emergency in which prolonged or multiple closely spaced seizures can result in long-term impairments.
- Conditions
- Patient Reported Outcomes, Patient Satisfaction, Long Term Outcomes, Status Epilepticus
- Trial name
- POSEIDON2 (NCT06100978)
- Where
- 19 sites in France
- Volunteers
- 145 people
- Sponsor
- Versailles Hospital
Multiple Myeloma, Patient Reported Outcome (PRO)
Digital Support for Multiple Myeloma Quality of Life
The objective of this prospective study is to investigate the quality of life of patients with multiple myeloma and the effectiveness of support provided through a personalized web-based platform.
- Conditions
- Multiple Myeloma, Patient Reported Outcome (PRO), Supportive Care in Cancer, Quality of Life
- Trial name
- DigiMyQoL (NCT07642362)
- Testing
- Digital support
- Where
- Greece
- Volunteers
- 108 people
- Sponsor
- CareAcross
Postoperative Recovery, Patient Reported Outcome Measures
QoR-15T in Cardiac Surgery
The objective of this prospective observational cohort study is to evaluate the validity, reliability, and responsiveness of the Turkish version of the Quality of Recovery-15 (QoR-15T) scale in adult patients undergoing elective…
- Trial name
- QoR15T-CARDİAC (NCT07593794)
- Where
- Turkey (Türkiye)
- Volunteers
- 150 people
- Sponsor
- Kocaeli City Hospital
Kidney Failure, Chronic, Frailty
Evolution of Physical Frailty and Patient-Reported Outcome Measures in Kidney Transplant Candidates: A Mixed-Methods Longitudinal Study Protocol
This study looks at how the physical and emotional health of people changes while they wait for a kidney transplant. Waiting for an organ can take a long time.
- Conditions
- Kidney Failure, Chronic, Frailty, Quality of Life, Kidney Transplantation
- Trial name
- NCT07607041
- Testing
- Longitudinal Frailty Assessment, Electronic Patient-Reported Outcome Measures (ePROMs)
- Volunteers
- 150 people
- Sponsor
- Hospital del Mar
Total Knee Anthroplasty, Patient Reported Outcome Measurements
Recovery Trajectories After Total Knee Arthroplasty
This prospective cohort study aimed to compare recovery trajectories following cruciate-retaining (CR) and posterior-stabilized (PS) total knee arthroplasty (TKA) using rehabilitation-centered patient-reported outcome measures…
- Conditions
- Total Knee Anthroplasty, Patient Reported Outcome Measurements, Cruciate Ligament Reconstruction
- Trial name
- NCT07595861
- Testing
- Cruciate-Retaining Total Knee Arthroplasty, Posterior-Stabilized Total Knee Arthroplasty
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Ondokuz Mayıs University
Patient Reported Outcome Measures, Colorectal Cancer
Predicting Disease Progression and/or Recurrence in Cancer
This is a prospective study addressing the challenge of predicting disease progression and/or recurrence in patients diagnosed with metastatic colorectal, pancreatobiliary, or esophagogastric cancer that are receiving anti-cancer…
- Conditions
- Patient Reported Outcome Measures, Colorectal Cancer, Pancreatic Cancer, Biliary Tract Cancer
- Trial name
- NCT04776837
- Testing
- Observational Cohort
- Where
- United States
- Volunteers
- 159 people
- Sponsor
- Massachusetts General Hospital
Patient Related Outcome Measures, Supportive Care
Screening for Supportive Care Needs of Oncological Patients and Professionals - Evaluation of a Short PRO-question Set
The systematic recording of patient-reported symptoms and health-related quality of life (patient-reported outcomes, PROs) is a central component of oncological care.
- Conditions
- Patient Related Outcome Measures, Supportive Care, Patient Reported Outcome (PRO)
- Trial name
- Scope-PRO (NCT07505498)
- Where
- Germany
- Volunteers
- 900 people
- Sponsor
- University Medical Center Goettingen
Deep Caries, Indirect Pulp Capping
Comparison Between Egyptian MTA, Biodentine Versus Calcium Hydroxide as Indirect Pulp Capping Materials In Permanent Teeth
Compare the clinical performance and patient satisfaction of Egyptian MTA, Biodentine versus Calcium Hydroxide as indirect pulp capping materials in permanent teeth
- Conditions
- Deep Caries, Indirect Pulp Capping, Mineral Trioxide Aggregate (MTA), Calcium Hydroxide
- Trial name
- NCT06683833
- Testing
- Egyptian MTA, Biodentine, Calcium Hydroxide (Ca(OH)2)
- Where
- Egypt
- Volunteers
- 35 people
- Sponsor
- Cairo University
Palliative Care, Palliative Care, Health Services
MultidISciplinary Care paThway tailoRed on frAilty in Cancer Patients Referred to Outpatient paLliative Care
The goal of this clinical trial is to learn whether a structured, Patient-Reported Outcome Measures (PROMs)-tailored palliative care pathway improves clinical outcomes and care experience in adults with advanced cancer referred…
- Conditions
- Palliative Care, Palliative Care, Health Services, Patient Reported Outcome (PRO), Patient Reported Outcome Measurements
- Trial name
- MISTRAL (NCT07469761)
- Testing
- Structured Palliative Care, Classical Palliative Care
- Where
- Italy
- Volunteers
- 120 people
- Sponsor
- Augusto Caraceni
Dental Plaque, Patient Reported Outcome
The Antiplaque and Antigingivitis Effect of Pure Green Tea Mouth Wash Compared to Placebo and Essential Oils Mouth Washes
The goal of this clinical trial is to to evaluate the antiplaque and antigingivitis effect of pure green tea mouthwash compared to placebo and essential oils mouthwashes in healthy patients.
- Conditions
- Dental Plaque, Patient Reported Outcome, Gingival Inflammation and Bleeding, Gingival Inflammation
- Trial name
- NCT07364565
- Testing
- Pure Green Tea Mouthwash, Listerine Total Care Mouthwash, Listerine Green Tea Mouthwash
- Where
- Jordan
- Volunteers
- 44 people, healthy volunteers welcome
- Sponsor
- King Abdullah University Hospital
Quality of Life, Patient Reported Outcome (PRO)
Patient-Reported Outcomes in Allogeneic Stem Cell Transplantation and CAR-T Therapy
3.1. Overview Prospective, multicenter, observational cohort study comparing short-term PROs measured with the HM-PRO between two exposure groups: patients undergoing allogeneic stem cell transplantation (allo-SCT) and patients…
- Conditions
- Quality of Life, Patient Reported Outcome (PRO), Allogeneic Blood and Marrow Transplantation (BMT), CAR T Cell Therapy
- Trial name
- QOL-ONE PRO-CT (NCT07289087)
- Volunteers
- 162 people
- Sponsor
- Associazione Qol-one
Lymphoma, B-Cell, Lymphoma, Hodgkin
STAY-STRONG Study of Exercise Training During Chemotherapy
This study evaluates the effectiveness of a supervised progressive resistance training program in patients malignant lymphomas with the primary outcome being lean body mass.
- Conditions
- Lymphoma, B-Cell, Lymphoma, Hodgkin, Exercise, Body Composition
- Trial name
- STAY-STRONG (NCT05556239)
- Testing
- Resistance Exercise Training
- Where
- Denmark
- Volunteers
- 42 people
- Sponsor
- Copenhagen University Hospital, Rigshospitalet