Pingree quant center trial#

Pingree S, Hawkins RP, Gustafson D, et al. Development, acceptance and use patterns of a computer based education and social support system for people living with AIDS/HIV infection. The quality of interactive computer use among HIV infected individuals. Smaglik P, Hawkins R, Pingree S, Gustafson D. Impact of a patient-centered, computer-based health information/support system. Gustafson DH, Hawkins RP, Boberg E, et al. Information needs, sources of information, and decisional roles in women with breast cancer. Patient participation in deciding breast cancer treatment and subsequent quality of life. Social support and breast cancer: a review. Nelles WB, McCaffrey RJ, Blanchard CG, Ruckdeschel JC. Enhancing cancer control: assessing cancer knowledge attitudes and beliefs in disadvantaged communities. An analysis of breast cancer coverage in selected women’s magazines, 1987–1995. Development of the Index of Medical Underservice. Recent trends in breast cancer mortality among white and black U.S. Quality of life research in oncology: past achievements and future priorities. Report from a National Cancer Institute (USA) workshop on quality of life assessment in cancer clinical trials. Nayfield SG, Ganz PA, Moinpour CM, Cella DF, Hailey BJ. Life after breast cancer: understanding women’s health-related quality of life and sexual functioning. Ganz PA, Rowland JH, Desmond K, Meyerowitz BE, Wyatt GE. Physical and psychosocial functioning and adjustment to breast cancer: long-term follow-up of a screening population. Vinokur AD, Threatt BA, Caplan RD, et al. Psychosocial correlates of breast cancer and its treatments. These benefits may be largest for currently underserved populations. In addition, experimental assignment interacted with several indicators of medical underservice (race, education, and lack of insurance), such that CHESS benefits were greater for the disadvantaged than the advantaged group.ĬONCLUSIONS: Computer-based patient support systems such as CHESS may benefit patients by providing information and social support, and increasing their participation in health care. At five-month follow-up, the CHESS group had significantly better social support and also greater information competence. At two-month follow-up, the CHESS group was significantly more competent at seeking information, more comfortable participating in care, and had greater confidence in doctor(s). MEASUREMENTS AND MAIN RESULTS: Pretest and two posttest surveys (at two- and five-month follow-up) measured aspects of participation in care, social/information support, and quality of life. INTERVENTIONS: Experimental group received Comprehensive Health Enhancement Support System (CHESS), a home-based computer system providing information, decision-making, and emotional support. PARTICIPANTS: Newly diagnosed breast cancer patients ( N=246) under age 60. The latter three sites treat many underserved patients. SETTING: Five sites: two teaching hospitals (Madison, Wis, and Chicago, Ill), two nonteaching hospitals (Chicago, Ill), and a cancer resource center (Indianapolis, Ind).

Pingree quant center trial#

OBJECTIVE: Assess impact of a computer-based patient support system on quality of life in younger women with breast cancer, with particular emphasis on assisting the underserved.ĭESIGN: Randomized controlled trial conducted between 19.