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442 studies found for:    patient-reported outcomes (PRO) cancer
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Rank Status Study
1 Recruiting Patient-Reported Outcomes Integrated in the Follow-up of Patients With Hematological Cancer
Intervention: Other: Completion of patient-reported outcome (PRO) questionnaires
Study Design: Allocation: Randomized;   Intervention Model: Parallel Assignment;   Masking: Care Provider;   Primary Purpose: Supportive Care
Number Enrolled: 225
2 Recruiting A Study of Patient-reported Outcomes in Patients With Lung or Esophageal Cancer
Intervention:
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 400
3 Completed Comprehensive Patient Reported Outcomes (PRO) Management for Oncology Practice
Intervention: Other: Report symptoms via web or phone-based system
Study Design: Allocation: Randomized;   Intervention Model: Crossover Assignment;   Masking: Open Label;   Primary Purpose: Supportive Care
Number Enrolled: 138
4 Completed Patient-Reported Outcomes Version of Common Terminology Criteria (CTCPRO) Cognitive Debriefing
Intervention: Behavioral: Interview
Study Design: Observational Model: Case-Only;   Time Perspective: Prospective
Number Enrolled: 20
5 Recruiting Patient Reported Outcomes Registry in Patient With Cancer Cachexia
Intervention:
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 250
6 Completed Patient-Reported Outcomes in Long-Term Survivors of Colon and Rectal Cancers
Intervention: Other: Telephone interview
Study Design: Observational Model: Cohort
Number Enrolled: 744
7 Unknown  A New Patient Reported Outcome Instrument to Assess Symptom Experience in Women With Vulvar Neoplasms (WOMAN-PRO)
Intervention:
Study Design:
Number Enrolled: 150
8 Recruiting Translation, Cross-cultural Adaptation and Validation of PRO-CTCAE for Italian-speaking Cancer Patients
Intervention:
Study Design: Observational Model: Case-Only;   Time Perspective: Cross-Sectional
Number Enrolled: 396
9 Active, not recruiting Validation Study of the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Intervention:
Study Design: Observational Model: Case-Only;   Time Perspective: Prospective
Number Enrolled: 1100
10 Recruiting Cervical Ca PROs in Clinical Practice
Interventions: Other: EORTC QLQ CX-24;   Other: Physician Feedback Form
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 100
11 Not yet recruiting PORTAL: Patient-reported Outcomes After Routine Treatment of Atypical Lesions
Intervention: Other: Survey
Study Design: Intervention Model: Single Group Assignment;   Masking: No masking;   Primary Purpose: Supportive Care
Number Enrolled: 1200
12 Recruiting Prospective PRO/QoL Registry for Patients With Bone Metastases of Breast or Prostate Cancer
Intervention:
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 500
13 Recruiting Evaluating the Use of Wearable Biosensors and PROs to Assess Performance Status in Patients With Cancer
Intervention: Device: Fitbit Charge HR®
Study Design: Intervention Model: Single Group Assignment;   Masking: Open Label
Number Enrolled: 40
14 Active, not recruiting Spanish Translation of the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Intervention: Behavioral: questionnaire administration followed by cognitive interviews
Study Design: Observational Model: Case-Only;   Time Perspective: Prospective
Number Enrolled: 120
15 Not yet recruiting Effect on Patient Reported Outcomes of VATS and SABR (LILAC)
Interventions: Other: EORTC QLQ-C30 (version 3.0).;   Other: PS Q18;   Other: Decision Self-Efficacy Scale
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 300
16 Completed Patient-Reported Outcomes (PRO)-Based Palliative and Hospice Care Practice: A Qualitative Study
Intervention: Behavioral: Interview
Study Design: Observational Model: Case-Only;   Time Perspective: Prospective
Number Enrolled: 9
17 Completed Web-based Patient Reported Outcome Measurement Information System (PROMIS ) to Explore Burden and Stress in Cancer Caregivers (BaSiC2)
Intervention:
Study Design: Time Perspective: Prospective
Number Enrolled: 172
18 Active, not recruiting Measuring Patient Satisfaction With Facial Appearance: Development and Validation of a New Patient-Reported Outcome Measure
Interventions: Other: questionnaire administration;   Procedure: assessment of therapy complications;   Procedure: psychosocial assessment and care;   Procedure: quality-of-life assessment
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 1745
19 Recruiting Johns Hopkins Breast Cancer Program Hormone Therapy Longitudinal Database
Interventions: Other: Sample collection;   Behavioral: Patient-reported outcomes
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Number Enrolled: 1000
20 Completed Bladder Cancer Patient-Reported Outcomes
Intervention:
Study Design: Observational Model: Cohort;   Time Perspective: Cross-Sectional
Number Enrolled: 108

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Study has passed its completion date and status has not been verified in more than two years.