Table 2.
Overview of all included studies sorted on outcome
| First author [reference], country, year | Design | Study population | HRQoL, anxiety and/or depression instrument | Information provision instrument | Results | Quality score |
| HRQoL | ||||||
| Frodj [12], Sweden, 2009 | Prospective | 36 carcinoid tumour patients | EORTC QLQ-C30 | CASC | Satisfaction with doctors’ provision of information was positively related to emotional function, global QoL at T1–T3 | 9 |
| Llewellyn [27], UK, 2006 | Prospective | 82 newly diagnosed head and neck cancer patients; 47% had an early stage (1 or 2) | General Health Survey Questionnaire, Short Form (SF-12) | SCIP | Satisfaction with information before treatment was predictive of mental component summary scores 6–8 months after the end of treatment, but not of physical component scores | 13 |
| Yu [35], China, 2001 | Prospective | 211 nasopharyngeal carcinoma patients; 41% had an early stage (I or II), 59% had a higher stage | FACT-G | Medical Interview Satisfaction Scale | More satisfaction with the medical information provided an average of 1 month after the end of radiotherapy had a better QoL 4 months later | 10 |
| Kerr [26], Germany, 2003 | Prospective | 980 breast cancer patients, 93.3% had an early stage (is, I, or II) | EORTC QLQ-C30; EORTC BR-23 (breast cancer specific) | Self-developed: satisfaction with hospital stay, doctor communication and aftercare | 17 QoL variables were significantly worse, up to 4 years after diagnosis, for those patients reporting unclear information | 11 |
| Vogel [36] Germany, 2009 | Prospective | 135 breast cancer patients | EORTC QLQ-C30 | Patient satisfaction with communication 25-item Likert scale; Self-developed question about level of information | Patients who rated their level of information at baseline as high experienced a higher QoL after 3 and 6 months | 10 |
| Griggs [21], USA, 2007 | Cross-sectional | 235 breast cancer patients | SF-36; IES | Self-developed: satisfaction with information | Strong positive relationship between satisfaction with information and vitality, mental health, and a strong negative relationship with distress | 9 |
| Mallinger [28], USA, 2005 | Cross-sectional | 182 breast cancer survivors | SF-36 | Information needs scale for recently diagnosed breast cancer patients | Better mental health is associated with greater satisfaction with information about treatment and survivorship | 10 |
| Davies [18], UK, 2008 | Cross-sectional | 102 breast cancer; 112 prostate cancer patients | FACT-G | Adapted version of the Information Satisfaction Questionnaire | Information satisfaction is a predictor of global QoL and its four dimensions. Satisfaction is positively associated with QoL | 9 |
| Annunziata [13], Italy, 1998 | Cross-sectional | 175 patients (breast, gastrointestinal, leukaemia, genitourinary tumours, lung, other neoplasms) | Functional Living Index for Cancer; State-Trait Anxiety Inventory | Degree of information on diagnosis and status of disease | Level of information did not affect QoL, satisfaction with information was associated with better QoL | 8 |
| Bredart [17], France, 2001 | Cross-sectional | 97 cancer patients with different diagnoses and stages | EORTC QLQ-C30 | CASC | Lower physical functioning and emotional functioning predicted higher satisfaction with doctor’s information provision | 11 |
| Elf [19], Sweden, 2001 | Cross-sectional | 30 cancer patients undergoing chemotherapy | EORTC QLQ-C30 | Self-developed: questions on patients’ satisfaction with information; Miller Behavioral Styles Scale | No significant differences in QoL could be found between satisfied and dissatisfied patients | 9 |
| Beckjord [16], USA, 2008 | Cross-sectional | 1040 cancer survivors (bladder, leukaemia, colorectal, non-Hodgkin’s lymphoma) | SF-36 | Self-developed: information needs | More information needs were associated with worse perceived mental and physical health | 8 |
| McInnes [29], USA, 2008 | Cross-sectional | 778 cancer survivors of six common cancers (bladder, breast, colorectal, prostate, uterine, melanoma); 3.1% in situ, 72.6% localised, 22.8% regional, 1.5% distant | SF-36 | Self-developed scales: information quality, information barriers, information needs | Worse physical and mental functioning was associated with greater need for information, worse ratings of information quality, and more barriers in obtaining information | 9 |
| Arora [14], USA, 2002 | Cross-sectional | 225 breast cancer patients; 80.4% had an early stage (is, I, or II) | Functional Assessment of Cancer Therapy (FACT) | Barriers to information access scale | Experience of greater barriers to accessing needed health information was significantly associated with lower emotional, functional and social/family well-being | 7 |
| Snyder [34], USA, 2007 | Cross-sectional | 117 cancer patients (breast, lung, prostate), 35.3% had an early stage, 14.7 locoregional, 50% metastatic | EORTC QLQ-C30 | Supportive Care Needs Survey | Better emotional function (not physical function) was associated with fewer unmet information needs | 7 |
| Anxiety and/or depression | ||||||
| Llewellyn [27], UK, 2006 | Prospective | 82 newly diagnosed head and neck cancer patients, 47% had an early stage (1 or 2) | HADS | SCIP | Satisfaction with information before treatment was predictive of depression 6–8 months after the end of treatment, but not of anxiety | 13 |
| Frodj [12],Sweden, 2009 | Prospective | 36 carcinoid tumour patients | HADS | CASC | Satisfaction with doctors’ provision of information was negatively related to anxiety and depression at T1–T3 | 9 |
| Vogel [36] Germany, 2009 | Prospective | 135 breast cancer patients | HADS | Patient satisfaction with communication 25 item Likert scale; self-developed question about level of information | Patients who rated their level of information at baseline as high were less depressed after 3 and 6 months | 10 |
| Sainio [33], Finland, 2003 | Cross-sectional | 273 cancer patients (81 breast, 73 haematological, 119 other); in 35%, cancer had recurred or metastases had appeared | Depression Scale | Self-developed questionnaire containing questions about obtained information and method of providing information | Both the respondents’ physical condition (positive) and depression (negative) were associated with receiving information | 9 |
| Jones [25], UK, 1999 | Cross-sectional | 525 cancer patients (309 breast, 129 prostate, 22 cervical, 65 laryngeal) | HADS | One question about satisfaction with information given | Depression was a predictor of dissatisfaction with information | 9 |
| Intervention studies | ||||||
| Haggmark [23], Sweden, 2001 | Prospective | 231 cancer patients (breast, bladder, prostate) | HADS; IES; Cancer Inventory of Problem Situations (CIPS II) | Self-developed: satisfaction with information questionnaire | No relation satisfaction and anxiety and depression | 10 |
| Molenaar [30], the Netherlands, 2001 | Prospective | 180 breast cancer patients | MOS20; EORTC QLQ-BR23 (breast cancer specific) | Self-developed: two instruments to measure satisfaction with information (general and treatment specific) | CDROM patients were more satisfied with breast cancer-specific information. At 3 and 9 months, a positive effect was found on general health. At 9 months, CDROM patients reported better physical functioning, less pain and fewer arm symptoms | 11 |
| Ong [31], the Netherlands, 2000 | Prospective | 201 cancer patients (gynaecologic or internal) | MOS20; Rotterdam Symptom Checklist | Patient Satisfaction Questionnaire | Patients provided with audio tape initial consultation were more satisfied than patients without the tape. The intervention did not have an effect on QoL | 10 |
| Hack [21], Canada, 2003 | Prospective | 628 breast cancer patients | Functional Assessment of Cancer Therapy (FACT-B); POMS | Patient Perception Scale | Audio tape of primary adjuvant treatment consultations to women with breast cancer was not significantly related to patient satisfaction with communication, mood state, or QoL at 12 weeks post-consultation and was not significantly affected by choice of receiving the audio tape | 10 |
| Hack [22], Canada, 2007 | Prospective | 425 prostate cancer patients; 76.2% had an early stage (I, or II), 14.6% had a high stage (III or IV) | Functional Assessment of Cancer Therapy (FACT-P); POMS | Patient Perception Scale | Audio tape of primary adjuvant treatment consultations to women with breast cancer was not significantly related to patient satisfaction with communication, mood state, or QoL at 12 weeks post-consultation and was not significantly affected by choice of receiving the audio tape | 11 |
| Iconomou [24], Greece, 2005 | Prospective | 145 cancer patients (lung, breast, colorectal, genitourinary, other); 50% had limited disease and 50% had advanced disease | EORTC-QLQ-C30; HADS | Single question about satisfaction with information provision | Patients provided with the information booklet reported significantly higher rates of satisfaction with information than control group, felt better and more informed, and perceived information received as being clearer and detailed. No significant benefits in anxiety, depression, QoL | 11 |
| Barlesi [15], France, 2008 | Prospective | 75 non-small-cell lung cancer patients | Psychologic Global Well-Being Index | Questionnaire of satisfaction of hospitalised patients; self-developed: question information satisfaction | No differences in QoL between non-small-cell lung cancer patients receiving oral information only as compared with oral plus written information | 10 |
| Passalacqua [32], Italy, 2009 | Prospective | 3197 cancer patients | HADS | One single question about satisfaction with received information | The per protocol analysis did show a reduction in psychological distress and dissatisfaction, for the patients in the PIS group compared to the control group, but differences were not significant | 9 |
CASC, Comprehensive Assessment of Satisfaction with Care; EORTC, European Organization for Research and Treatment of Cancer; FACT, Functional Assessment of Cancer Therapy; HADS, Hospital Anxiety and Depression Scale; HRQoL, health-related quality of life; SCIP, Satisfaction with information profile; IES, Impact of Event Scale; SF-36, Medical Outcomes Study Short Form 36; MOS20, Medical Outcomes Study 20; PIS, Point of Information and Support; POMS, Profile of Mood States.