To evaluate outlook, an intervention to assist patients address emotional and existential needs, in people living with advanced disease yet not in the final months of life. If improvements were demonstrated, it could improve understanding of intervention in early versus late palliative care contexts.

Three-arm randomized controlled trial testing the effect of Outlook, with an attention control (RM) and a true control (usual care UC). Baseline interview completed in person or on the phone, then randomized 1:1:1. Participants assigned to Outlook were interviewed in person three times during a one-month period after the baseline interview. Session 1 was life review; session 2 was issues of forgiveness, regret, things left unsaid, or undone; and session 3 was heritage and legacy. Interviews were a week apart and lasted 45 minutes. Participants assigned to RM met with the interventionist in person three times during a one-month period and listed to a relaxation CD for 40 minutes. UC participants were not contacted. Interventionists were clinical social workers trained in delivering standardized interventions following a manualized script. Sessions were audio recorded.

• N = 221   
• AGE: Mean = 67.8 years
• MALES: 96%  
• FEMALES: 4%
• CURRENT TREATMENT: Not applicable
• KEY DISEASE CHARACTERISTICS: Advanced cancer, congestive heart failure, chronic obstructive pulmonary disease, end-stage renal disease, end-stage liver disease
• OTHER KEY SAMPLE CHARACTERISTICS: Non-hospice eligible, veterans

• SITE: Single site   
• SETTING TYPE: Outpatient    
• LOCATION: Durham, North Carolina

• PHASE OF CARE: Active anti-tumor treatment
• APPLICATIONS:  Elder care, palliative care

Three-arm randomized controlled trial testing the effect of Outlook compared with an attention control (relaxation meditation [RM]) and a true control (usual care [UC]) on patient QOL, functional status, and emotional well-being.

Primary outcomes:

• Preparation and completion: QUAL-E a 31-item validated measure of QOL at the end of life

Secondary outcomes:

• Anxiety: Brief Profile of Mood States
• Depression: Center for Epidemiological Studies-Depression scale
• Quality of Life: FACT-General FACT
• Spiritual Well Being: Functional Assessment of Chronic Illness Therapy-spiritual well-being.

The study compared change in primary and secondary outcomes over time between outlook and both the RM and UC groups. Outlook participants had higher improvements in mean preparation (p = 0.02) and mean completion (p = 0.04) at five week follow-up compared with UC. The differences did not persist for the seven week follow-up. Compared to the RM group, Outlook participants did not have a significant difference in preparation and completion at either follow up. Outlook social well-being was improved over RM at the seven-week follow-up. Outlook did not show significant difference over time in QOL, anxiety, or depression. Qualitative interview participants (15%) described Outlook at helpful. Participants valued the opportunity to review life memories as a source of strength and to identify unresolved issues.

Outlook did not demonstrate sustained improvements in preparation, anxiety, or depression and overall QOL compared to RM in adults with advanced illness who were not hospice eligible. Outlook as an intervention was positive for patient quality of life in reviewing memories as a source of strength, and releasing unresolved emotions and concerns.

• Baseline sample/group differences of import
• Risk of bias (no appropriate attentional control condition)  
• Risk of bias (sample characteristics)
• Key sample group differences that could influence results

The structured Outlook intervention which assists patients to review and resolve important life issues and concerns is valuable for patients with terminal illness, including patients with cancer. Nurses can assess patients for distress and ensure that opportunities and referrals with support resources are explored. This would be relevant to the hospice setting.

To evaluate the effects of a web-based social networking and coping skills training intervention on cancer-related patient based outcomes: distress, depression, anxiety, and psychological well-being. Secondary outcomes are vigor and fatigue.

Participants initially completed a baseline survey following which they were given access to the online health space intervention or waitlisted for the intervention (waitlist control group) randomly. Intervention included an evidence-based online distress management intervention for a period of 12 weeks, including modules, chats, discussion boards, and web mails.

• N = 347   
• AGE: Treatment group, mean = 52.9 years; waitlist control group, mean = 53.1 years; all combined, mean = 53.1 years
• MALES: 21%; n = 73
• FEMALES: 79%; n = 274
• CURRENT TREATMENT: Other
• KEY DISEASE CHARACTERISTICS: Multiple tumors: Most common were breast cancer (n = 161, 46.4%) followed by prostate cancer (n = 43, 12.4%)
• OTHER KEY SAMPLE CHARACTERISTICS: Participants with multiple cancers and participants with female reproductive cancers were at 6.1% each (n = 21)

• SITE: Multi-site (tumor registry, outreach to websites, and cancer forums)
• SETTING TYPE: Other (online)
• LOCATION: Online

PHASE OF CARE: Multiple phases of care

Randomized controlled clinical trial

• Primary outcomes: distress measured by Distress Thermometer, psychological functioning by Outcomes questionnaire-45, depression by Center for Epidemiologic Studies Depression scale, and trauma-related anxiety by Impact of Event Scale-revised 
• Secondary outcomes: Fatigue and vigor by the subscales from Profile of Mood States (POM-SF) 
• Engagement on outcomes: Time spent online with the intervention  
• Outcomes measured at baseline and 12 weeks.

No baseline difference was noted between the intervention and control group in terms of demographic and clinical characteristics. All the five outcomes improved over time, but no significant difference between the treatment and control group for psychological functioning, depression, anxiety, and vigor. Interaction between time and treatment group fatigue (time fatigue declined in the treatment group compared to control group). No significant reduction in distress and depression between the groups, although it reduced within the groups over time, association between intervention and engagement.

Health space social networking did not improve the cancer-related distress outcomes.

• Unintended interventions or applicable interventions not described that would influence results
• Questionable protocol fidelity
• Subject withdrawals ≥ 10%  
• Other limitations/explanation: Attrition

Online interventions could be suggested to patients as it is associated with strong engagement.

To determine the feasibility and effectiveness of an individual, nurse-navigator intervention for relieving distress, anxiety, depression, and health-related quality of life in women newly diagnosed with breast cancer.

Symptom screening and counseling by nurse navigator; specific intervention described in detail in prior paper.

• N = 50   
• AGE: Mean age = 55 in control group and mean age = 50 in intervention group
• FEMALES: 100%
• CURRENT TREATMENT: Not applicable
• KEY DISEASE CHARACTERISTICS: Breast cancer

• SITE: Single site   
• SETTING TYPE: Outpatient    
• LOCATION: Copenhagen, Denmark

PHASE OF CARE: Multiple phases of care

Randomized, interventional pilot study with outcomes assessed at baseline, 6 months, and 12 months

Distress Thermometer; Hospital Anxiety and Depression Scale; European Organisation for Research and Treatment of Cancer QLQ-C30

Women in the intervention group reported significantly greater satisfaction with treatment and rehabilitation and lower levels of distress, anxiety, and depression after 12 months. No significant effects on health-related quality of life were noted.

Individually tailored nurse navigation intervention resulted in statistically significant lower levels of distress, anxiety, and depression.

Small sample (< 100)

Oncology nurses are in a key position to screen for distress in women with breast cancer. Patients with high levels of distress may benefit from individually tailored counseling to decrease distress, anxiety, and depression.

Evaluate the effects of music therapy in addition to standard treatment in patients undergoing high-dose chemotherapy (HDC) plus autologous stem cell transplantation (ASCT) on quality of life, anxiety, and depression.

For the intervention group, a trained music therapist administered therapy two times per week for at least 20 minutes, based on the individual needs of each patient established prior to therapy, and each session included a debrief or aftertalk. Quality of life was assessed prior to therapy, weekly during treatment, at discharge, and again three months later.

• N = 66   
• AGE: Mean = 50 years (all older than 18 years)
• MALES: 43 
• FEMALES: 23 
• CURRENT TREATMENT: Chemotherapy, other
• KEY DISEASE CHARACTERISTICS: Malignancies treated with HDC plus ASCT with an expected inpatient stay of two weeks or longer
• OTHER KEY SAMPLE CHARACTERISTICS: No evidence of participation in other clinical trials, immobilization, brain metastasis, experiencing a severe psychotic episode, or having major depression. Seventy percent of patients in the intervention group had multiple myeloma versus 40% in the control group

• SITE: Single site   
• SETTING TYPE: Inpatient    
• LOCATION: Department of Oncology and Hematology of the University Medical center Hamburg-Eppendorf, Germany

• PHASE OF CARE: Active anti-tumor treatment
• APPLICATIONS: Elder care

Randomized controlled trial

EORTC QLQ-C30, HADS-D, Karnofsky performance score

Quality of life declined less in the intervention group (8.1 points) versus control (11.4 points), difference between groups was not significant (p = 0.394)

Because of multiple limitations of study, the authors declared their findings to be preliminary.

• Small sample (< 100)
• Baseline sample/group differences of import
• Selective outcomes reporting
• Measurement validity/reliability questionable
• Subject withdrawals ≥ 10%  
• Other limitations/explanation: 29 of the 66 patients involved in the study were assessed in follow up (high dropout rate); extracted data from the large number of patients with multiple myeloma to report positive effects of music therapy, but when this data was considered, results were no longer significant.

Opportunity for further research