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. Author manuscript; available in PMC: 2018 Mar 1.
Published in final edited form as: Contemp Clin Trials. 2017 Jan 16;54:98–104. doi: 10.1016/j.cct.2017.01.005

Table 2.

Patient- and caregiver-reported outcome measures.

Outcome Participant Measure Description
Quality of Life
Primary Outcome
Patient FACIT-PAL
Functional Assessment of Chronic Illness Therapy -- Palliative Care
Measures physical, social, emotional, & functional well-being with a palliative care subscale developed to identify quality of life concerns for patients with advanced cancer [31-33]
Symptom Burden Patient ESAS
Edmonton Symptom Assessment Scale
Patient-rated symptom scale developed & validated in cancer patients receiving palliative care [27, 28, 34]
Self-efficacy Patient Cancer Behavior Inventory-Brief version Measures self-efficacy for coping with cancer [35]
Patient-oncologist Relationship Patient Human Connection Scale Measures therapeutic alliance between patients with advanced cancer and their physicians [36]
Distress Patient NCCN Distress Thermometer Measures distress in patients with cancer on a 0-10 scale [29]
Hope Patient and Caregiver Herth Hope Index Abbreviated instrument to assess hope in adults in clinical settings [37]
Mood Patient and Caregiver HADS
Hospital Anxiety and Depression Scale
Measures symptoms of anxiety & depression, extensively validated for screening emotional distress among advanced cancer patients and family members [38-41]
Caregiver Burden Caregiver Zarit Burden Interview – Short version Self-report of burden experienced while providing care to a loved one, shorter version of widely used measure [42]
Self-efficacy Caregiver Caregiver Inventory A measure of self-efficacy for caregivers; includes assessment of self-care and communication [43]
Satisfaction Caregiver FAMCARE-2 Measures family caregiver satisfaction with care in a variety of palliative care settings [44, 45]