Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03307200
Other study ID # EC/2017/0350
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 3, 2017
Est. completion date August 27, 2021

Study information

Verified date January 2023
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Nowadays, high-quality cancer care is more than just diagnosis and treatment of cancer. Healthcare must respond to the specific needs of the patients to provide patient-centered care. To date, research on the unmet supportive care needs in bladder cancer patients undergoing radical cystectomy is scarce. Because the needs of the patients may differ according to the phase in the illness trajectory, it is important that prospective research is carried out. Research in other cancer populations shows that unmet supportive care needs are negatively associated with health-related quality of life, psychological distress, physical activity and the health literacy of the patient. By incorporating the above factors into this study, we can not only map the unmet supportive care needs of the patient, but also explore possible associations between the variables. Since this is the first prospective study on supportive care needs in bladder cancer, this is a hypothesis-generating study.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date August 27, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age is 18 years or older - Patients diagnosed with bladder cancer who will undergo radical cystectomy - Patient has to be able to sign informed consent Exclusion Criteria: - Metastatic cancer - Presence of a second primary tumor with the exception of fully deleted prostate cancer, non-melanoma skin tumor or tumor diagnosed = 5 years ago and under control

Study Design


Locations

Country Name City State
Belgium Ghent University Ghent
Belgium University Hospitals Leuven Leuven

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Unmet supportive care needs Assessed with the 34-item supportive care needs survey (SCNS-34) From baseline up to 1 year
Secondary Change in Cancer-specific Health-related quality of life Assessed with the EORTC-qlq-c30 From baseline up to 1 year
Secondary Change in Bladder cancer-specific Health-related quality of life Assessed with the EORTC-qlq-blm30 From baseline up to 1 year
Secondary Change in Psychological distress Assessed with the distress thermometer From baseline up to 1 year
Secondary Change in problems associated with psychological distress Assessed with the problem list From baseline up to 1 year
Secondary Health literacy Assessed with the BRIEF Health Literacy Screening Tool Baseline
Secondary Change in Physical activity pattern Assessed with the Godin Leisure-Time Exercise Questionnaire From baseline up to 1 year
Secondary Change in Physical Activity Stage of change Assessed with a questionnaire based on an algorithm made by Marcus et al. From baseline up to 1 year
Secondary Change in The use of health care services Separate questions where the patient is asked about his/her use of supportive health care services. From baseline up to 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT05583916 - Same Day Discharge for Video-Assisted Thoracoscopic Surgery (VATS) Lung Surgery N/A
Completed NCT04448041 - CRANE Feasibility Study: Nutritional Intervention for Patients Undergoing Cancer Surgery in Low- and Middle-Income Countries
Completed NCT03213314 - HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies N/A
Enrolling by invitation NCT05534490 - Surgery and Functionality in Older Adults N/A
Recruiting NCT04792983 - Cognition and the Immunology of Postoperative Outcomes
Terminated NCT04612491 - Pre-operative Consultation on Patient Anxiety and First-time Mohs Micrographic Surgery
Recruiting NCT06397287 - PROM Project Urology
Recruiting NCT04444544 - Quality of Life and High-Risk Abdominal Cancer Surgery
Completed NCT04204785 - Noise in the OR at Induction: Patient and Anesthesiologists Perceptions N/A
Completed NCT03432429 - Real Time Tissue Characterisation Using Mass Spectrometry REI-EXCISE iKnife Study
Completed NCT04176822 - Designing Animated Movie for Preoperative Period N/A
Recruiting NCT05370404 - Prescribing vs. Recommending Over-The-Counter (PROTECT) Analgesics for Patients With Postoperative Pain: N/A
Not yet recruiting NCT05467319 - Ferric Derisomaltose/Iron Isomaltoside and Outcomes in the Recovery of Gynecologic Oncology ERAS Phase 3
Recruiting NCT04602429 - Children's Acute Surgical Abdomen Programme
Completed NCT03124901 - Accuracy of Noninvasive Pulse Oximeter Measurement of Hemoglobin for Rainbow DCI Sensor N/A
Completed NCT04595695 - The Effect of Clear Masks in Improving Patient Relationships N/A
Recruiting NCT06103136 - Maestro 1.0 Post-Market Registry
Completed NCT05346588 - THRIVE Feasibility Trial Phase 3
Completed NCT04059328 - Novel Surgical Checklists for Gynecologic Laparoscopy in Haiti
Recruiting NCT03697278 - Monitoring Postoperative Patient-controlled Analgesia (PCA) N/A