Atkinson NL Massett HA Mylks C Hanna B Deering MJ Hesse BW (2007) User-centered research on breast cancer patient needs and preferences of an internet-based clinical trial matching system. J Med Internet Res9: e13.
2.
Broom A (2005) Virtually He@lthy: a study into the impact of Internet use on disease experience and the doctor/patient relationship. Qual Health Res15: 325–345.
3.
Cox K McGarry J (2003) Why patients don't take part in cancer clinical trials: an overview of the literature. Eur J Cancer Care12: 114–122.
4.
Eysenbach G (2003) The impact of the internet on cancer outcomes. CA Cancer J Clin53: 356–371.
5.
Fayter D McDaid C Ritchie G Stirk L Eastwood A (2006) A Systematic Review of Barriers, Modifiers and Benefits Involved in Participation in Cancer Clinical Trials.York: Centre for Reviews and Dissemination.
6.
Kivits J (2006) Informed patients and the internet. A mediated context for consultations with health professionals. J Health Psychol11: 269–282.
7.
Krishnasamy M (1996) Social support and the patient with cancer: a consideration of the literature. J Adv Nurs23: 757–762.
8.
Lindsay J (2005) Getting the numbers: the unacknowledged work in recruiting for survey research. Field Methods17: 119–128.
9.
Mapstone J Elbourne D Roberts IG (2007) Strategies to improve recruitment to research studies. Cochrane Database Syst Rev Issue2: MR000013 10.1002/14651858.MR000013.pub3.
10.
McDonald AM Knight RC Campbell MK Entwistle VA Grant AM Cook JA (2006) What influences recruitment to randomised controlled trials? A review of trials funded by two UK funding agencies. Trials7: 9.
11.
Rozmovits L Ziebland S (2004) What do patients with prostate or breast cancer want from an Internet site? A qualitative study of information needs. Patient Educ Couns53: 57–64.
12.
Satterlund M McCaul L Sandgren A (2003) Information gathering over time by breast cancer patients. J Med Internet Res5: e15.
13.
Stevenson F Kerr C Murray E Nazareth I (2007) Information from the internet and the doctor-patient relationship: the patient perspective - a qualitative study. BMC Fam Pract8: 47.
14.
Thornton H Dixon Woods M (2002) Recruitment of women into trials. Lancet359: 164.
15.
Till JE (2003) Evaluation of support groups for women with breast cancer: importance of the navigator role. Health Qual Life Outcomes1: 16.
16.
Tomaka J Thompson S Palacios R (2006) The relation of social isolation, loneliness, and social support to disease outcomes among the elderly. J Aging Health18: 359–384.
17.
Watson JM Torgerson DJ (2006) Increasing recruitment to randomised trials: a review of randomised controlled trials. BMC Med Res Methodol6: 34.
18.
Wells M Harrow A Donnan P Davey P Devereux S Little G (2004) Patient, carer and health service outcomes of nurse-led early discharge after breast cancer surgery: a randomised controlled trial. Br J Cancer91: 651–658.
19.
Ziebland S Chapple A Dumelow C Evans J Prinjha S Rozmovits L (2004) How the internet affects patients' experience of cancer: a qualitative study. BMJ328: 564.