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Patient Participation clinical trials

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NCT ID: NCT02615769 Completed - Lung Diseases Clinical Trials

Effect on Attendance if Including Focused Information of Spirometry in Preventive Health Checks

Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if focused information of spirometry in the invitation to preventive health checks will increase the attendance compared with a standard invitation to preventive health checks.

NCT ID: NCT02401919 Recruiting - Communication Clinical Trials

Basic Care Revisited_Communication for Patient Participation

BCR_C
Start date: May 2014
Phase: N/A
Study type: Interventional

COMMUNICATION - Feasibility and effectiveness 'Tell-us Cards' in hospital patients - Objective - To investigate the feasibility and effectiveness of 'Tell-us Cards' on patient participation in basic care in hospital settings. - Design - Cluster randomised controlled early trial design (Phase 2B, MRC Framework). Patients of two surgical and two medical wards (n=140) will be included in this study. Before and after the introduction of the intervention, assessments will take place in patients and nurses at these wards. - Intervention - The 'Tell-us card' is a tool to elicit patients preferences and needs in basic care. Patients are invited to write down their specific questions and concerns. The cards are handed out to patients admitted to the hospital (daily). Patients and informal caregivers are invited to use the cards to state their preferences. Nurses are instructed to use the cards as a tool in their dialogue with the patient in making care plans, during ward rounds or for discharge information sessions. - Comparison - Usual care - Primary outcome - Patient perception of participation in care (Individualized Care Scale (ICS) - Secondary - Use and content of the 'Tell-us Cards' actions taken by nurses as a consequence of what patients 'tell them' by means of the 'Tell-us Cards', Quality from the Patients' perspective (QPP), EQ-5D, and CQ satisfaction with communication & care in general

NCT ID: NCT01183156 Unknown status - Colorectal Cancer Clinical Trials

Re-invitation to Screening Colonoscopy: a Randomized Study

REINVITE
Start date: August 2010
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of reminding letter and educational intervention on attendance to screening colonoscopy in nonresponders to initial invitation to screening colonoscopy.

NCT ID: NCT00985907 Terminated - Multiple Myeloma Clinical Trials

Doxil® + Melphalan + Velcade (DMV) in Relapsed/Refractory Multiple Myeloma

DMV
Start date: October 28, 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The median overall survival (OS) of relapsed/refractory multiple myeloma (MM) is less than nine months. However, phase II data with the proteasome inhibitor bortezomib (Velcade®) has been heartening, with 35% overall response rates and median survival of 16 months. In-vitro data has shown that this agent dramatically increases the sensitivity to chemotherapeutic agents. Liposomal doxorubicin (Doxil), melphalan, and bortezomib all have different mechanisms of action and toxicity profiles. Clinical studies employing two drug combinations with these agents in patients with refractory MM have found favorable efficacy (nearly no progression of disease) and tolerance data. Thus, the investigators are initiating a phase I/II study to examine the safety and efficacy of combining all three agents into the regimen DMV (Doxil® + melphalan + Velcade).