N/A
N=374
Pre-consultation Compassion Among Patients Referred to a Cancer Center
Cancer · Anxiety · Compassion · Empathy
Bottom Line
View on ClinicalTrials.gov: NCT04503681 ↗Enrolled (actual)
374
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcome: Primary: Anxiety Subscale of the Hospital Anxiety and Depression Scale (HADS) — 7; 7 score on a scale — p=0.473
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Enhanced compassion video (Other); Standard introduction video (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- The Cooper Health System
- Primary completion
- Oct 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Anxiety Subscale of the Hospital Anxiety and Depression Scale (HADS) |
7; 7 | 0.473 |
| SECONDARY Depression Subscale of the Hospital Anxiety and Depression Scale |
3; 3 | 0.338 |
Summary
Patients diagnosed with cancer commonly have a high degree of anxiety during an initial oncology consultation, which may interfere with a patient's ability to retain information required to make informed treatment decisions. A previous study randomized breast cancer survivors (volunteers) to view either (a) a brief video depicting a standard initial consultation from an oncologist or (b) an identical consultation with the addition of compassionate statements from the oncologist, and found the compassionate statements reduced anxiety among the volunteers. However, it is currently unknown if watching a video containing compassionate statements from an oncologist prior to an actual initial oncology consultation will reduce anxiety among patients referred to a cancer center. The aim of this randomized control trial is to test if watching a brief video containing compassionate statements from an oncologist, compared to watching a standard introduction video, prior to an initial oncology consultation will reduce the degree of anxiety among patients referred to a cancer center.
This is a prospective, randomized controlled clinical trial at an academic cancer center. The investigators will enroll adult patients scheduled for an initial oncology consultation. Subjects will be randomly assigned to receive a "standard introduction video" or "enhanced compassion video" for viewing prior to the initial oncology consultation. On arrival to the cancer center anxiety severity will be measured using the Hospital Anxiety and Depression scale (HADS). The HADS has two 7-item subscales (HADS Anxiety and HADS Depression) and is well-validated among oncology patients. Wilcoxon rank-sum test will be used to test for a difference in the HADS subscales between the two video groups.
Eligibility Criteria
Inclusion Criteria
- age ≥ 18 years
- scheduled for an initial oncology consultation
Exclusion Criteria
- patients who do not have an active email address or are medically unable to complete the research questionnaire at the time of the initial cancer consultation.
Data sourced from ClinicalTrials.gov (NCT04503681). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.