- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06395831
Assessment of Quality of Life and Independence, as Well as Received Social Support for Spinal Cancer.
Assessment of Quality of Life and Independence, as Well as Received Social Support in Patients Before and After Surgery for Spinal Cancer
- Evaluation of the quality of life of patients before and after surgery for benign and malignant spinal cancers, assessing whether it depends on the size of the tumor, type of cancer, malignancy and its location
- evaluation of patients' independence before and after surgery for benign and malignant spinal tumors, evaluation of what factors influenced patients' different independence
- multidimensional assessment of perceived social support of patients before and after surgery for benign and malignant spinal cancers, taking into account three sources of support: significant person, family and friends
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
RESEARCH PROJECT DESCRIPTION, RESEARCH METHODOLOGY:
Research objectives:
- To evaluate the quality of life of patients before and after surgery for benign and malignant spinal cancers, to assess whether it depends on the size of the tumor, type of cancer, malignancy and its location
- evaluation of patients' independence before and after surgery for benign and malignant spinal tumors, assessment of what factors influenced patients' different independence
- multidimensional evaluation of perceived social support of patients before and after surgery for benign and malignant spinal cancers, taking into account three sources of support: significant person, family and friends
Scientific (research) problems:
- What is the quality of life of patients before and after surgery for benign and malignant spinal cancers ? Is the quality of life in patients with spinal cancer dependent on tumor size, malignancy, location or type of cancer ?
- How do patients rate their independence both before and after surgery for spinal cancers at different stages of the disease?
- How do patients with spinal cancer at different stages of the disease rate the social support they received both before and after surgery?
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Edyta Laska
- Phone Number: +48692430150
- Email: elaska@afm.edu.pl
Study Locations
-
-
Lesserpoland
-
Krakow, Lesserpoland, Poland, 30-693
- Recruiting
- St. Raphael's Hospital
-
Contact:
- Edyta Laska, Ph.
- Phone Number: +48692430150
- Email: elaska@afm.edu.pl
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria for the study:
-clinical diagnosis of spinal cancer
Study exclusion criteria:
-inflammatory and disc disease of the spinal column
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life assessed using The World Health Organization Quality of Life (WHOQOL) scale. Social support assessed using Zimet's Multidimensional Perceived Social Support Scale - the original version on the MSPSS.
Time Frame: 12 months to 24 months
|
Quality of life assessed using The World Health Organization Quality of Life (WHOQOL-BREF) scale questionnaire which contains 26 questions analyzing four domains of life and separately perception of quality of life and self-assessment of health status. It is used to assess the quality of life of both healthy and sick people in clinical practice and addresses the following domains of quality of life: somatic functioning, psychological functioning, social functioning and community functioning. Social support assessed using Zimet's Multidimensional Perceived Social Support Scale - the original version on the MSPSS. The Multidimensional Scale of Perceived Social Support takes into account the multidimensionality of perceived social support, considering three primary sources of support: significant other, family and friends. The scale consists of 12 statements, which the subject addresses using a seven-point Likert scale, where 1 means "strongly disagree" and 7 means "strongly agree." |
12 months to 24 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 32/2023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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