Anxiety Clinical Trial
Official title:
Mindfulness Interventions and Cutaneous T Cell Lymphoma (CTCL)
The primary objective is to assess the feasibly, adherence, and effects of mindfulness-based
stress reduction (MBSR) on anxiety and health-related quality of life in adult patients with
cutaneous T-cell lymphoma at the Yale Cancer Center/Smilow Cancer Hospital.
Participants will attend group sessions led by an instructor experienced in MBSR in an
academic setting. The mindfulness meditation group sessions will take place at the Smilow
Cancer Center at the Yale New-Haven Hospital.
Participants will attend weekly 2.5-hour group sessions (of 10-14 persons) based on the
standard mindfulness-based stress reduction (MBSR) protocol. Participants will be assigned
home practice based on the MBSR protocol, and will be given audio recordings (MP3) to
accompany and instruct in home practice.
Eligible participants will attend weekly group sessions for 8 weeks and will be assessed at
baseline, following cessation of the intervention (8-weeks), and 16 weeks. Outcomes will be
assessed at baseline, 8 weeks, and 16 weeks. Extended effects of the intervention will be
assessed at 16 weeks.
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