Breast Cancer Clinical Trial
Official title:
Hypnosis for Hot Flashes in Breast Cancer Survivors
RATIONALE: Hypnosis may be effective in decreasing hot flashes in breast cancer survivors.
PURPOSE: This randomized clinical trial is studying how well hypnosis works in treating hot
flashes in breast cancer survivors.
OBJECTIVES:
- Determine the efficacy of hypnosis in controlling hot flashes in women who are breast
cancer survivors.
- Determine the extent to which hypnotizability is related to the success of the
hypnotherapy intervention.
OUTLINE: This is a randomized, controlled study. Patients are stratified according to age,
gender, race, and educational background. All patients complete a Hot Flash Daily Diary to
record frequency and severity of hot flashes for 1 week. Patients are then randomized to 1
of 2 treatment arms.
- Arm I (hypnotherapy): Patients undergo hypnotherapy once a week for 5 weeks. Patients
complete the Hot Flash-Related Daily Interference Scale, the Hospital Depression and
Anxiety Sub-scale, the CES Depression Scale, and the MOS-Sleep and Sexual Function
Scales in week 5 after the last hypnotherapy intervention. Patients also complete
another Hot Flash Daily Diary for 1 week in week 6 and are administered the Stanford
Hypnotic Clinical Scale in week 7.
- Arm II (control): Patients receive no contact for 4 weeks. Patients complete the
questionnaires as in arm I in week 5. Patients also complete another Hot Flash Daily
Diary for 1 week in week 6 and are administered the Stanford Hypnotic Clinical Scale in
week 7.
PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.
;
Allocation: Randomized, Primary Purpose: Supportive Care
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