Clinical trials: Patient Satisfaction
Guided Imagery
The Effect of Guided Imagery on Activity-Specific Balance Confidence, Pain, and Psychological Well-Being
The aim of this clinical trial is to evaluate the effect of guided imagery on activity-specific balance confidence, pain, and psychological well-being in elderly orthopedic patients.
- Trial name
- NCT06855927
- Testing
- Guided Imagery
- Volunteers
- 78 people
- Sponsor
- Inonu University
User Experience, Postoperative Complications
Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures
The goal of this prospective, international multi-centre pilot study is to assess the functionality and user experience of a new vital sign monitoring system in 20 patients and 20 nurses in the general ward at each centre.
- Conditions
- User Experience, Postoperative Complications, Acute Medical Conditions
- Trial name
- NCT06289699
- Where
- 5 sites in United States, Germany and 3 more
- Volunteers
- 100 people
- Sponsor
- Christian S. Meyhoff
Satisfaction, Dentist-Patient Relations
Socioeconomic Profile and Patient Satisfaction Assessment
The aim of the study was to evaluate the socioeconomic patient's profile and their level of satisfaction in the general dental practice clinic.
- Trial name
- Satisfaction (NCT00690599)
- Where
- Brazil
- Volunteers
- 80 people
- Sponsor
- Fortaleza University
Well-Being, Psychological
Virtue-Based vs. Cognitive-Behavioral Interventions in Patients With Chronic Medical Disease
The aim of this study is to analyze the specific and common mechanisms of change of two active treatments, one based on reducing barriers -Cognitive Behavioral Therapy (CBT)- and the other based on enhance resources -Virtue-Based…
- Trial name
- NCT06501235
- Testing
- Cognitive-Behavioral Therapy (CBT), Virtue-Based Intervention (VBI)
- Where
- Spain
- Volunteers
- 100 people
- Sponsor
- University of Valencia
Ambulatory Surgical Procedures, Anxiety Disorders
Educational Video and Peri-operative Anxiety
Preoperative anxiety is a common problem with an impact on surgical outcome, anaesthetic drug dosage and patient's satisfaction. An important component of preoperative anxiety is due to concerns related to anaesthesia.
- Trial name
- NCT03581097
- Testing
- Video Group
- Where
- Switzerland
- Volunteers
- 93 people
- Sponsor
- University Hospital, Geneva
Balance, Lower Limb
Effect of Ballet Course on Lower Limb Strength, Balance, Working Memory and the Compliance and Satisfaction
In recent years, sports have become popular, and major gyms or private exercise studios have been opened continuously. A dazzling array of course content allows students to choose according to their preferences.
- Conditions
- Balance, Lower Limb, Strength, Working Memory
- Trial name
- NCT05683587
- Testing
- ballet course, strength course
- Where
- Taiwan
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Kaohsiung Medical University Chung-Ho Memorial Hospital
Knee Osteoarthristis
BFR Training and Knee Osteoarthritis
Knee osteoarthritis (KOA) is a chronic, progressive degenerative joint disease characterized by cartilage and bone degeneration, synovial inflammation, and structural changes.
- Trial name
- NCT07590323
- Testing
- Standard Treatment, Pain neuroscience education, Blood flow restriction training
- Where
- Saudi Arabia
- Volunteers
- 90 people
- Sponsor
- University of Hail
Breastfeeding Education, Maternal Self-Efficacy
Mixed Reality as a Health Literacy Strategy for Breastfeeding Education
The goal of this randomized controlled trial is to evaluate whether a mixed reality-based educational strategy improves breastfeeding satisfaction and self-efficacy in pregnant women compared to traditional counseling.
- Conditions
- Breastfeeding Education, Maternal Self-Efficacy, Breastfeeding Satisfaction
- Trial name
- NCT06800521
- Testing
- Mixed Reality Breastfeeding Education, Traditional Breastfeeding Counseling
- Where
- Colombia
- Volunteers
- 68 people, healthy volunteers welcome
- Sponsor
- Universidad de la Sabana
Pain, Satisfaction, Patient
Lidocaine Spray vs Viscous Lidocaine Solution Plus Lidocaine Spray in Patients Undergoing Non-Sedated EGD
This study aimed to compare the efficacy of lidocaine spray (S) alone versus lidocaine spray combined with lidocaine viscous solution (S+V) in facilitating pharyngeal observation during Non-sedating upper gastrointestinal…
- Trial name
- NCT06185933
- Testing
- Lidocaine Spray, Lidocaine Viscous+Lidocane spray
- Where
- Thailand
- Volunteers
- 250 people
- Sponsor
- Sawanpracharak hospital
Survival of the Implants With Revision as Endpoint, Clinical Performance With HHS
Primary Uncemented Partly Ti-coated Total Hip Prosthesis With and Without HA, and Alumina-on-alumina Articulation
Both HA coated and certain uncoated femoral stems have good results in general. On the cup side the results are more variable, either with or without HA.
- Conditions
- Survival of the Implants With Revision as Endpoint, Clinical Performance With HHS, Patients Satisfaction With the Hip Implant
- Trial name
- NCT01118247
- Testing
- Uncemented primary total hip arthroplasty
- Where
- Norway
- Volunteers
- 400 people
- Sponsor
- University Hospital of North Norway
Mastectomy, Postoperative Pain
The Use of an Acellular Dermal Matrix in a Two-Staged Breast Reconstruction
This study intends to compare postoperative outcomes of a tissue expander placement following a mastectomy with two different operative techniques.
- Conditions
- Mastectomy, Postoperative Pain, Complications
- Trial name
- NCT00616824
- Testing
- Dermamatrix to cover lateral aspect of tissue expander, Serratus anterior to cover lateral aspect of tissue expander
- Where
- United States
- Volunteers
- 36 people
- Sponsor
- Vanderbilt University Medical Center
Shade Match
Shade Match, Marginal Adaptation and Patient Satisfaction of VITA ENAMIC multiColor Versus IPS e.Max CAD Veneers
It is assumed that there will be no difference in shade match, marginal adaptation and patient satisfaction between VITA ENAMIC multiColor and IPS e.max CAD anterior laminate veneers.
- Trial name
- NCT04774614
- Testing
- anterior laminate veneers
- Volunteers
- 21 people, healthy volunteers welcome
- Sponsor
- Cairo University
Bone Loss
Crestal Bone Loss and Patient Satisfaction of Screw Retained Restoration
On of the main fixed prosthetic options of completely edentulous patients is the screw-retained implant supported prosthesis which was constructed on transmucosal abutments with its encountered problems such as: hardness to make…
- Trial name
- NCT03671668
- Testing
- titanium bases using intra oral luting cement technique
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Cairo University
Labor, Induced, Patient Preference
Should I Have an Elective Induction?
The goal of the proposed study is to perform a pilot test of a patient-centered decision support tool to help pregnant people and providers work together in making informed, shared decisions regarding whether or not to opt for…
- Trial name
- SELECTION (NCT05838313)
- Testing
- Elective Induction of Labor Decision Support Tool
- Where
- 2 sites in United States
- Volunteers
- 66 people, healthy volunteers welcome
- Sponsor
- University of South Florida
Patient Satisfaction
Study of Comparative Effectiveness of Prucalopride and Lubiprostone in Constipation Predominant Irritable Bowel Syndrome
This will be a semi-experimental study on constipation predominant IBS patient. One group of patient will receive prucalopride 2mg daily and another group of patient will receive lubiprostone 8 microgram twice daily.
- Trial name
- NCT04985669
- Testing
- Prucalopride 2mg
- Where
- Bangladesh
- Volunteers
- 140 people
- Sponsor
- Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Urologic Cancer, Satisfaction, Patient
Telemedicine for Postoperative Follow-up After Oncological Surgeries
The study will be a prospective, randomized, non-inferiority, open-label study, to be carried out at the Cancer Institute of the State of São Paulo for 6 months and will include patients agreeing to voluntary participation upon…
- Conditions
- Urologic Cancer, Satisfaction, Patient, Surgery, Postoperative Adhesion
- Trial name
- NCT06282354
- Testing
- Type of post-operative appointment
- Volunteers
- 200 people
- Sponsor
- Instituto do Cancer do Estado de São Paulo
Headaches
Telemedicine Versus Traditional Specialist Consultation for Headache: a Non-inferiority Trial
Headache is a frequent cause of visits to the GPs office, and the investigators have previously shown that this group accounts for about 20 % of patients referred to a general neurologic outpatient clinic.
- Trial name
- VHS (NCT02270177)
- Testing
- Telemedicine, videoconsultation
- Where
- Norway
- Volunteers
- 402 people
- Sponsor
- University Hospital of North Norway
Patient Engagement, Patient Preference
Increasing Decision Quality for Men With Lower Urinary Tract Symptoms
In this study, the investigators show that by upskilling of primary care physicians (PCPs) in SDM and leveraging on a novel pictorial Visual Analogue Uroflowmetry Score (VAUS), they can enhance older men's recognition of LUTS and…
- Trial name
- NCT04851275
- Testing
- Physicians trained in shared decision making, Physicians were not trained in shared decision making
- Where
- Singapore
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- SingHealth Polyclinics
Breast Cancer
Drain Removal on Postoperative Safety and Patient Satisfaction in R-E-NSM With Prepectoral DIBR
Breast cancer is a malignant tumor that seriously threatens the health of women, with an increasing incidence rate. The current main treatment methods include multidisciplinary diagnosis and treatment such as surgery…
- Trial name
- DRAIN (NCT07237828)
- Testing
- Drain Removal Timing After Endoscopic Breast Reconstruction Surgery
- Where
- China
- Volunteers
- 379 people
- Sponsor
- Du Zhenggui
Presbyopia Correction, Presbyopia
Clinical Evaluation of Visual Performance, Spectacle Independence, and Patient Satisfaction With TECNIS PureSee Mini-Monovision and TECNIS PureSee-TECNIS Odyssey Mix-Match
The purpose of the study is to evaluate the binocular clinical endpoints of distance, intermediate, and near vision and patient reported outcomes utilizing mini-monovision versus mix-match approaches for the correction of…
- Conditions
- Presbyopia Correction, Presbyopia, Dysphotopsia, Visual Acuity
- Trial name
- NCT07860567
- Testing
- TECNIS PureSee IOL (Model DEN00V/DET150), TECNIS Odyssey IOL (Model DRN00V/DRT150)
- Where
- United States
- Volunteers
- 68 people
- Sponsor
- Dr. Daniel H. Chang, MD