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. 2018 Oct 26;33(1):5–23. doi: 10.1177/0269216318809582

Table 1.

Description of the included randomised controlled trials.

Study Settinga Study design Intervention versus control Participants characteristics Outcomesb (measurement tools)
El-Jawahri et al.39
USA
OC Parallel-group randomised controlled trial 6-min video with verbal narrative of goals-of-care versus verbal narrative of goals-of-care 50 patients with malignant glioma
Cancer type:
Malignant giloma
Ethnicity:
White: 92%
Education:
Higher education (university and postgraduate): 66%
Patient-reported:
Patients’ preference for cardiopulmonary resuscitation (intervention 8.7% vs control 40.7%; p= 0.02, SDQ), patients’ knowledge of cardiopulmonary resuscitation (SDQ), patients’ uncertainty of decision-making (DCS), patients’ comfort, helpful and recommendation level with the video (SDQ)
Process:
None applicable
Epstein et al.38
USA
OC Pilot randomised controlled trial 3-min video decision aids with image of cardiopulmonary resuscitation and mechanical ventilation versus verbal narrative about cardiopulmonary resuscitation and mechanical ventilation 56 patients with progressive pancreas or hepatobiliary cancer
Cancer type (top 3):
1. Exocrine pancreas Carcinoma (78.6%)
2. Cholangiocarcinoma (8.9%)
3. Hepatocellular carcinoma (5.4%)
Ethnicity:
White: 62.5%
Education:
Higher education (university and postgraduate): 80.4%
Patient-reported:
Study impressions (SDQ), patients’ preference for cardiopulmonary resuscitation (SDQ), patients’ knowledge of cardiopulmonary resuscitation (SDQ)
Process:
Completion of advance care planning (intervention 40% vs control 15%; OR= 3.6, 95% CI 0.9–18.0; p= 0.07, MR), deaths occurred (MR), the number of patients died in hospice setting (MR)
Volandes et al.42
USA
OC Parallel-group randomised controlled trial 3-min video depicting a patient on a ventilator and cardiopulmonary resuscitation being performed on a stimulated patient versus verbal narrative describing cardiopulmonary resuscitation 150 patients with advanced cancer
Cancer type (top 3):
1. Lung (23.3%)
1. Colon (23.3%)
2. Breast (11.3%)
Ethnicity:
White: 47.3%
Education:
Higher education (university and postgraduate): 44.6%
Patient-reported:
Patients’ preference for cardiopulmonary resuscitation (intervention 20% vs control 48%, OR= 3.5, 95% CI 1.77.2; p< 0.001, SDQ), patients’ knowledge of cardiopulmonary resuscitation (SDQ), patient’s perception of watching video (SDQ)
Process:
None applicable
Jones et al.45
UK
OC, HOC Feasibility randomised controlled trial Meeting with a trained medical staff using a checklist of topic domains versus usual care 77 patients with recurrent advanced cancer
Cancer type (top 3):
1. Bowel (14.3%)
2. Prostate (13%)
3. Gynaecological (10.4%)
Ethnicity:
White: 92.1%
Education:
Higher education (university and postgraduate): 62%
Patient-reported:
Willingness to discuss about future (coefficient 0.7, 95%CI -1.9-3.2; p= 0.611, VAS), happiness with communication (VAS), degree of satisfaction of care (VAS), anxiety and depression (HADS)
Process:
None applicable
Stein et al.43
Australia
HOT Parallel-group randomised controlled trial A semi-structured discussion with a psychologist using a pamphlet called ‘Living with Advanced Cancer’ versus usual care 120 patients with metastatic cancer who were no longer being treated with
curative intent
Cancer type (top 3):
1. Colorectal (26.7%)
2. Other (25%)
3. Lung (16.7%)
Ethnicity:
None stated
Education:
Higher education (university and postgraduate): 76.6%
Patient-reported:
Depression and anxiety (HADS), patients’ knowledge of cardiopulmonary resuscitation (SDQ)
Process:
Hospital death (intervention 19% vs control 50%, 95% CI 11%–50%; p= 0.004, MR), whether a patient had a do not resuscitation order (MR), the number of days between the earliest do not resuscitation order documentation and death (MR), caregiver burden/(CRA)
Clayton et al.37
Australia
PCC Parallel-group randomised controlled trial Provision of a question prompt list to patients before consultation with physicians versus standard consultation 174 patients with an advanced progressive life limiting illness
Cancer type (top 3):
1. Gastrointestinal (37.9%)
2. Other (22.4%)
3. Lung (20.1%)
Ethnicity:
None stated
Education:
Higher education (university and postgraduate): 39%
Patient-reported:
Discussion about prognosis and end-of-life care (ratio 2.3; 95% CI, 1.7–3.2; p< 0.0001, coding), achievement of patient information needs (CISQ), satisfaction with the consultation (SDQ), anxiety (SSAI)
Process:
Physician satisfaction with communication during the consultation (SDQ), consultation duration (coding)
Rodenbach et al.41
USA
OC Cluster randomised controlled trial A communication coaching with a question prompt list for patients before the consultation with oncologist versus usual care 180 patients who had advanced non-hematologic cancer
Cancer type:
None stated
Ethnicity:
White: 83.9%
Education:
Higher education (university and postgraduate): 61.1%
Patient-reported:
Discussion about prognosis and end-of-life care (intervention 70.2% vs control 32.6%; p< 0.001, coding)
Process:
None applicable
Epstein et al.40
USA
OC, CC, HOT Cluster randomised controlled trial Values and options in cancer care (VOICE) versus usual care 265 Patients had either stage IV non-hematologic cancer or stage III cancer and whose physician ‘would not be surprised’ if the patient were to die within 12 months.
Cancer type:
1. Aggressive cancer
2. Less aggressive
Ethnicity:
White: 88.7%
Education:
Higher education (university and postgraduate): 72.5%
Patient-reported:
Physician-patient communication (intervention effect,0.34; 95% CI,0.06–0.62; p= 0.02, APPC, VR-CoDES, PTCC and FPI), quality of life (FACT-G, McGill QOL)
Process:
Utilisation of aggressive treatment in the last 30 days of life (MR), hospice utilisation (MR), intervention fidelity (SDQ)
Walczak et al.44
Australia
CC Parallel-group randomised controlled trial Communication support programme versus usual care 110 patients with advanced, incurable cancer
Cancer type (top 3):
1. Lung (16.4%)
2. Prostate (15.5%)
3. Bowel/anus (11.8%)
Ethnicity:
None stated
Education:
Higher education (university and postgraduate): 62%
Patient-reported:
Discussion about future (intervention 1.0 vs control 0.6; p= 0.028, coding), communication self-efficacy (PEPPI), preference for information and decision-making (CISQ), quality-of-life (FACT-G, McGill QOL scale), satisfaction of intervention (SDQ)
Process:
Consultation length (SDQ), intervention fidelity (SDQ)
a

Setting: OC: oncology clinic; HOC: hospice; CC: cancer centre; PCC: palliative care centre; HOT: hospital; HC: home care organization; MC: managed care organisation.

b

Outcomes (measurement tools): SDQ: self-developed questionnaire; MR: medical records; VAS: Visual Analogue Scale; HADS: Hospital Anxiety and Depression Survey; DCS: Decisional Conflict Scale; PEPPI: Perceived Efficacy in Physician/Patient Interactions Scale; CISQ: Cassileth Information Styles Questionnaire; FACT-G: Function Assessment of Cancer Therapy: General; McGill QOL: McGill Quality of Life Questionnaire; SSAI: Spielberger State Anxiety Inventory; CRA: Caregivers Reaction Assessment; APPC: The Active Patient Participation Coding; VR-CoDES: The Verona VR-CoDES system; PTCC: the prognostic and treatment choices; FPI: The Framing of Prognostic Information Scale.

Italics indicate primary outcome if multiple outcomes were evaluated.

Key to colour coding.

Inline graphic Single-element intervention – video decision aids.

Inline graphic Single-element intervention – written information materials.

Inline graphic Multiple-elements intervention – written information materials + communication coaching.

Inline graphic Multiple-elements intervention – video decision aids + written information materials + communication coaching.