Symptom clusters and their effect on the functional status of patients with cancer.
M J Dodd, C Miaskowski, S M Paul
https://pubmed.ncbi.nlm.nih.gov/11338755/Actively Recruiting
Led by WellSpan Health · Updated on 2026-03-02
1000
Participants Needed
5
Research Sites
43 weeks
Total Duration
Cancer affects millions worldwide and can greatly impact survival and daily quality of life. Treatments like surgery, chemotherapy, and radiation may cause side effects such as fatigue, pain, and neuropathy, which influence physical functioning, emotional health, and social interactions. Researchers are working to better understand the full impact of cancer and its treatments on patients lives by developing a patient-centered quality of life QOL survey tailored for individuals with cancer. This study focuses on creating and using a specialized QOL survey that captures what matters most to cancer patients by directly involving them in sharing their experiences. It plans to observe patients diagnosed with primary cancer within the past 6 months and will analyze differences in quality of life among groups based on race, ethnicity, and gender. The study is observational and does not involve experimental treatments. Participants will be followed over time with assessments at baseline, 6, 12, 18, and 24 months to evaluate quality of life differences. They will complete questionnaires reflecting their physical, emotional, and social well-being. The study aims to provide insights to help patients, families, and healthcare providers better address needs and improve supportive care throughout the cancer journey. Participation involves signing informed consent and completing quality of life surveys over two years.
CONDITIONS
WellSpan-THRIVE Cancer QOL Study
J
Joan K Moore, MSN, RN, OCN, CCRP
R
Rahul Kashyap, MBBS, MBA, FCCM
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WellSpan Health
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual)
Duration - Baseline assessment at enrollment
Participants complete a patient-centered quality of life survey tailored specifically for cancer patients to capture factors affecting their quality of life.
1 baseline visit (in-person or virtual)
Duration - Up to 24 months
Participants are monitored over time with repeated quality of life assessments to understand differences based on race, ethnicity, and gender.
Assessments at 6, 12, 18, and 24 months (in-person or virtual)
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Lead Sponsor