People are “participants” in research

BMJ

Volumn 318, Issue 7191, 1999, Pages 1141-

  Chalmers, Iain ^a   Jackson, William ^b   Carvel, David ^c  

^a UK COCHRANE CENTRE   (United Kingdom)

^b The Old Chapel   (United States)

^c NONE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CONTROLLED CLINICAL TRIAL; HUMAN; NOMENCLATURE; NOTE; PATIENT;

CONTROLLED CLINICAL TRIALS; HUMANS; PATIENTS; TERMINOLOGY;

EID: 85007729500     PISSN: 09598138     EISSN: 14685833     Source Type: Journal    
DOI: 10.1136/bmj.318.7191.1141a     Document Type: Letter

References (8)

1. Boynton PM. People should participate in, not be subjects of, research. BMJ 1998; 317: 1521. (28 November.)
2. Consumers for Ethics in Research. Newsletter 1989;No 1.
3. Chalmers I. What do I want from health research and researchers when I am a patient? BMJ 1995; 310: 1315–1318.
4. British Psychological Society. Code of conduct and ethical principles. London: BPS, 1991: 5.
5. Boynton PM. People should participate in, not be subjects of, research. BMJ 1998; 317: 1521. (28 November.)
6. Standing Advisory Group on Consumer Involvement in the NHS Research and Development Programme. Aims and values. Leeds: NHS Executive, 1998.
7. Minerva. BMJ 1996; 313: 240.
8. Boynton PM. People should participate in, not be subjects of, research. BMJ 1998; 317: 1521. (28 November.)