Clinical trials: Study Protocol Feasibility
Stroke, Parkinson Disease
Feasibility of Two New Software Modules for the Rehabilitation of Patients With Neuromuscular Upper Limb Impairments
Introduction: In the recent past, medical training systems using virtual reality (VR) have been introduced to neurorehabilitation to train motor function deficits in patients.
- Conditions
- Stroke, Parkinson Disease, Traumatic Brain Injury, Guillain-Barre Syndrome
- Trial name
- NCT03268304
- Testing
- VR-based training including AO and MI
- Sponsor
- Reha Rheinfelden
Breast Cancer Early Stage Breast Cancer (Stage 1-3), Breast Neoplasm Malignant Female
Supervised Exercise During Neoadjuvant Chemotherapy for Breast Cancer
The goal of this clinical trial is to learn whether supervised exercise is practical and safe for women receiving chemotherapy before surgery for breast cancer.
- Trial name
- NCT07764341
- Testing
- Supervised exercise
- Where
- Bahrain
- Volunteers
- 80 people
- Sponsor
- King Hamad University Hospital, Bahrain
Vasomotor Symptoms Associated With Menopause
A Feasibility Study of a Group Talking Therapy Programme for NHS Staff With Menopausal Hot Flushes and Night Sweats.
The goal of this feasibility study/clinical trial is to evaluate the feasibility and acceptability of a CBT group programme (MENOS protocol) for hot flushes and night sweats for National Health Service (in The United Kingdom)…
- Trial name
- NCT07759830
- Testing
- Cognitive Behavioral therapy group programme for Menopausal Hot flushes and Night Sweats, No intervention
- Where
- United Kingdom
- Volunteers
- 35 people
- Sponsor
- Queen's University, Belfast
Depressive Disorder, Major
Dexmedetomidine Adjuvant Treatment for Depressed Patients Undergoing ECT
Major depressive disorder (MDD) is a highly prevalent and disabling condition for which the currently available treatments are not fully effective.
- Trial name
- NCT04661475
- Testing
- Dexmedetomidine Injection [Precedex], Normal saline
- Volunteers
- 76 people
- Sponsor
- Sultan Qaboos University
Fibromyalgia
PRPP Model for Evaluation the Effect of Non-pharmaceutical Therapies
To assess the application of partially randomized patient preference (PRPP) trial model which concerns the patients' preference on evaluation the therapeutic effect of non-pharmaceutical therapy, and to observe the therapeutic…
- Trial name
- NCT01869712
- Testing
- Cupping therapy, Acupuncture
- Where
- China
- Volunteers
- 126 people
- Sponsor
- Beijing University of Chinese Medicine
Heart Failure, Advance Care Planning
Advance Care Planning in Patients With Heart Failure in Denmark
Advance care planning (ACP) represents a process whereby a patient, in consultation with healthcare professionals, family members and important others, makes decisions about his or her future healthcare and wishes for end-of-life…
- Conditions
- Heart Failure, Advance Care Planning, Communication, Feasibility Studies
- Trial name
- DanHFacp (NCT05269875)
- Testing
- ACP
- Where
- Denmark
- Volunteers
- 20 people
- Sponsor
- Nordsjaellands Hospital
Post-Acute COVID-19 Syndrome, Biofeedback, Psychology
Prevention of Long Covid Syndrome
Biofeedback equipment is classified by the Food and Drug Administration (FDA) as medical device class II and this type of equipment/treatment has shown evidence regarding stress management in post-Covid-19 syndrome.
- Conditions
- Post-Acute COVID-19 Syndrome, Biofeedback, Psychology, Quality of Life, Depressive Symptoms
- Trial name
- NCT05793736
- Testing
- Biofeedback training, Treatment as usual
- Where
- Italy
- Volunteers
- 17 people
- Sponsor
- University of Cagliari
Unspecified Adult Solid Tumor, Protocol Specific
Palliative Care Intervention in Patients With Solid Tumors Participating in Phase I Clinical Trials
Patients enrolled in phase I clinical trials could potentially benefit from palliative care concurrently, yet limited evidence is available to support such a change in care.
- Trial name
- NCT01612598
- Testing
- counseling intervention, quality-of-life assessment, questionnaire administration
- Where
- 2 sites in United States
- Volunteers
- 16 people
- Sponsor
- City of Hope Medical Center
Chronic Obstructive Pulmonary Disease
Evaluating the Feasibility, Acceptability and Pre Testing the Impact of a Self-management and Tele Monitoring Program for COPD Patients in Lebanon
Chronic obstructive pulmonary disease (COPD) has a significant impact on quality of life and is costly to the health care system.
- Trial name
- NCT04196699
- Testing
- self-management program
- Volunteers
- 30 people
- Sponsor
- University of Paris 13
Breast Cancer
Management of Cognitive Difficulties After Cancer Treatments in Women Treated for Breast Cancer: Feasibility Study (Step 1 of the Cog-Stim Protocol)
Investigator general objective is therefore to study and compare the benefit of several methods of management of cognitive difficulties reported by patients during treatment for breast cancer, among several treatments, offered…
- Trial name
- COG STIM (NCT04213365)
- Testing
- Cognitive stimulation sessions coupled with Adapted Physical Activity sessions.
- Where
- France
- Volunteers
- 20 people
- Sponsor
- Centre Francois Baclesse
Nutritional Deficiency
A Cardiac Surgery Virtual Nutrition Intervention Program Feasibility Study-VIP Study Protocol
This feasibility study will look to identify the impact that a remote/virtual nutritional intervention can have on nutrition literacy and knowledge retention of the cardiac surgery patient.
- Trial name
- NCT05183607
- Testing
- Virtual Nutrition Education
- Where
- Canada
- Volunteers
- 20 people
- Sponsor
- St. Boniface Hospital
Radiculopathy Lumbar, Disk Herniated Lumbar
Position-Induced Opening of the Intervertebral Foramen is Efficient to Treat an Acute Lumbosacral Radiculopathy Caused by Disc Herniation
Efficiency of the conservative mechanical lumbosacral nerve root decompression, as an adjunct to pharmacological treatment, in the case of acute lumbosacral radiculopathy.
- Conditions
- Radiculopathy Lumbar, Disk Herniated Lumbar, Low Back Pain
- Trial name
- NCT04276519
- Testing
- Physiotherapeutic, non-invasive position-induced opening of the intervertebral foramen
- Volunteers
- 20 people
- Sponsor
- General Hospital Sveti Duh
Ileus Postoperative, Nasogastric Tube
Feasibility and Safety of an Ileus Management Protocol for Postoperative Ileus After Abdominal Surgery
The goal of this clinical trial is to evaluate whether a standardized treatment algorithm, the Ileus Management Protocol (I-MAP), is feasible and safe for the management of patients who develop postoperative ileus (POI) within 30…
- Trial name
- NCT07194525
- Testing
- A standardized treatment algorithm for postoperative ileus after abdominal surgery, based on nasogastric tube output and including stepwise use of water-soluble contrast, imaging, and prokinetic medic
- Where
- Switzerland
- Volunteers
- 60 people
- Sponsor
- University of Lausanne Hospitals
Depression, Anxiety
Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress
The aims of this study are to test the effectiveness and acceptability of internet-delivered treatment for depression, anxiety and stress in university students.
- Conditions
- Depression, Anxiety, Stress
- Trial name
- EAITDAS (NCT02614443)
- Testing
- Space from Depression, Space from Anxiety, Space from Stress
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Silver Cloud Health
Heart Failure, Self-care
mHealth Intervention to Support Self-care During the Hospital to Home Transition in Individuals With Heart Failure
This study is a pilot randomized controlled trial designed to evaluate the feasibility, acceptability, usability, and preliminary efficacy of a mobile health (mHealth) educational self-management intervention for individuals with…
- Conditions
- Heart Failure, Self-care, Transitional Care
- Trial name
- HF-mHealth (NCT07478081)
- Testing
- mHealth Educational Self-Management Application, Usual transitional care
- Where
- Colombia
- Volunteers
- 30 people
- Sponsor
- Universidad de la Sabana
Hypertension, Dyslipidemia
A Novel Digital Tool Clinicians Can Use to Prescribe Exercise to Patients With Cardiovascular Disease Risk Factors
The investigators will conduct a feasibility and pilot efficacy randomized controlled trial to test the usability and user satisfaction of an evidence-based digital health tool the investigators developed for clinicians to use to…
- Conditions
- Hypertension, Dyslipidemia, Diabetes Mellitus, Obesity
- Trial name
- P3-EX (NCT07238556)
- Testing
- Experimental - 12 Week P3-EX Unsupervised Exercise Program with Virtual Weekly Oversight from Graduate Research Assistants, Active Control - 12 Week ACSM-PAVS Unsupervised Exercise Program with Virtual Weekly Oversight from Graduate Research Assistants
- Where
- 3 sites in United States
- Volunteers
- 72 people
- Sponsor
- University of Connecticut
Bacterial Vaginosis, Fungal Vaginal Infections
Clinical Protocol CERN Feasibility Study
The goal of this clinical trial is to learn if the intravaginal Cern device works to treat bacterial vaginosis and fungal vaginitis in premenopausal women. It will also learn about the safety of the device.
- Trial name
- NCT06933420
- Testing
- Cern Device
- Where
- 3 sites in United States
- Volunteers
- 9 people
- Sponsor
- Cern Corporation
T4 Colorectal Cancer, ERAS
Feasibility of ERAS Protocol in T4 Colorectal Cancer Patients
Patients diagnosed with T4 colorectal cancer represent a specific subgroup of colorectal patients, frequently composed of fragile patients whose advanced nature of the disease often requires a multi organ resection by an open…
- Conditions
- T4 Colorectal Cancer, ERAS, Colon Cancer, Fast Track Protocol
- Trial name
- NCT04466696
- Testing
- ERAS protocol
- Volunteers
- 82 people
- Sponsor
- University of Rome Tor Vergata
HIV Prevention and Care
Lafiya HIV Self-testing Study Protocol
The study aims to address low testing and related issues such as stigma, low-risk perception, and concerns about confidentiality affecting testing.
- Trial name
- NCT06238323
- Testing
- LAFIYA
- Where
- Ghana
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- University of Rochester
Intracranial Aneurysms
Canadian eCLIPs™ Safety and Feasibility Study Protocol
The purpose of this study is to evaluate the safety and feasibility of the eCLIPs™ Family of Products for the treatment of unruptured intracranial bifurcation aneurysms in conjunction with embolization coils.
- Trial name
- CESIS (NCT01957683)
- Testing
- eCLIPs™ Family of Products
- Where
- 5 sites in Canada
- Sponsor
- Evasc Medical Systems Corp.