Renal Transplant Recipients Clinical Trial
Official title:
Implementing eHealth Interventions Into Regular Clinical Practice to Enhance Care Planning, Communication and Patient Involvement
The purpose with this study is to test a digital patient-provider communication tool for symptom and needs management among patients with chronic health conditions.
Living with chronic health conditions affects all areas of life. Fatigue, sleeping problems, pain and loneliness are common. In addition to troublesome symptoms that vary in intensity, many experience worry and uncertainty. There is a need to improve the quality of follow-up of patients with chronic health conditions. A digital patient-provider communication tool, which supports shared decision making, can be one way to improve quality. The digital tool (InvolveMe) will provide patients with the opportunity to complete and submit a symptom and need assessment prior to out-patient visits at the hospital. Also, patients will have the opportunity to use secure e-mail for follow-up from health care providers in between hospital visits. The assessment will allow patient to prioritize what is important to talk with their health care providers about. Such a tool can help to make changes in symptoms more visible to both patients and health care providers, as well as make it easier to ask for information and guidance to deal with the individual difficulties patients' experience. The goal is to better address symptoms and concerns and to enhance follow up and coordination between consultations as well as increase the quality of life and reduce illness related stress. The digital communication tool will first be tested in a feasibility pilot study. The tool will be offered to 50 patients (kidney transplant recipients and patients with non-functioning pituitary adenomas). Participants will be given the opportunity to use the digital communication tool with baseline measures and following measures after 3 and 6 months. After pilot testing of the tool, a larger longitudinal clinical study among 160 patients with non-functioning pituitary adenomas (n=60) and kidney transplant recipients (n=100) will be conducted to assess the clinical utility. The participants will be assigned to use the digital communication tool, and will be followed with repeated measures over 12 months. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT02956005 -
Envarsus XR in African American Renal Transplant Recipients
|
N/A | |
Completed |
NCT01086904 -
Safety and Efficacy of an Inactivated and Non Adjuvanted Vaccine Against Influenza A in Renal Transplant Recipients
|
Phase 2 | |
Completed |
NCT00319189 -
Efficacy and Safety of Nateglinide Treatment in Renal Transplant Recipients
|
Phase 4 | |
Completed |
NCT01859832 -
Validation of a Novel Diagnostic Tool for the Evaluation of Post Renal Transplant Immunosuppression: The ImmuKnow Assay
|
N/A | |
Recruiting |
NCT03110406 -
Effects of Whole-body Vibration Training on the Heart Rate Variability Cardiac in Kidney Transplantation
|
N/A | |
Recruiting |
NCT02973464 -
The Strategy in the Prevention of Renal Post-transplant Cytomegalovirus Infection Among Chinese Population
|
Phase 3 | |
Active, not recruiting |
NCT03797196 -
RCT Comparing Immunosuppressive Regimens in Elderly Renal Transplant Recipients
|
Phase 4 | |
Terminated |
NCT01318915 -
Research Study of ATG and Rituximab in Renal Transplantation
|
Early Phase 1 | |
Recruiting |
NCT00327483 -
Web Based Renal Transplant Patient Medication Education
|
Phase 4 | |
Terminated |
NCT00271830 -
Sexual Function in Male Renal Transplant Patients
|
N/A | |
Completed |
NCT00138970 -
Calcineurin Inhibitor-Free Immunosuppression in Renal Transplant Recipients at Low Immunogenic Risk
|
Phase 4 | |
Withdrawn |
NCT04903054 -
Selective CD28 Blockade in Renal Transplant Recipients
|
Phase 2 | |
Completed |
NCT02706678 -
Efficacy and Safety Study of the Switch From Cyclosporin to Tacrolimus in Renal Transplant Recipients
|
Phase 4 | |
Recruiting |
NCT03726307 -
Allogeneic Regulatory Dendritic Cell (DCreg) Renal Study
|
Phase 1 |