Clinical Trials Directory

Trials / Completed

CompletedNCT00903474

Mindful Movement Program in Improving Quality of Life in Older Female Breast Cancer Survivors

Mindful Movement Program for Breast Cancer Survivors

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
49 (actual)
Sponsor
City of Hope Medical Center · Academic / Other
Sex
Female
Age
50 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Mindful movement is a self-directed activity of mindfulness (intention, attention, and attitude) and physical movement. A mindful movement program may be effective in improving well-being in older women who are breast cancer survivors. PURPOSE: This randomized clinical trial is studying how well a mindful movement program works in improving quality of life in older female breast cancer survivors.

Detailed description

OBJECTIVES: * To test the effects of the 12-week Mindful Movement Program on quality of life in older female breast cancer survivors. * To test the effects of this program on mindfulness outcomes in these participants. * To compare mindfulness qualities in the experimental group with the control group. * To determine the qualitative benefits of this program as described by these participants. OUTLINE: Participants are randomized to 1 of 2 intervention arms. * Arm I (Mindful Movement Program \[MMP\]): Participants undergo a 2-hour MMP session once weekly for 12 weeks. Participants are encouraged to practice intentional-mindful movement at home 5 minutes daily during weeks 1-4, 10 minutes daily during weeks 5-8, and 15 minutes daily during weeks 9-12. Mindful movement is a self-directed activity incorporating mindfulness concepts and physical movement. Mindfulness consists of the three core elements: intention (reasons for participating in a mindfulness intervention), attention (observing experiences in the present moment), and attitude (nonjudgmental openness and acceptance of experiences). Each MMP session includes verbal sharing with a partner and the group and movement individually and with a partner, while focusing on the elements of mindfulness. Music is incorporated into some portion of each session. * Arm II (control): Participants undergo no intervention. All participants complete questionnaires for sociodemographic and individual characteristics, quality of life (including psychological, social, spiritual, and physical well-being, anxiety and depression, fear of recurrence, body image, and upper body symptoms), movement, and mindfulness (including attention, self-compassion, and intention) at baseline and weeks 12 and 18. PROJECTED ACCRUAL: A total of 75 participants (45 in the experimental group and 30 in the control group) will be accrued for this study.

Conditions

Interventions

TypeNameDescription
OTHERquestionnaire administration
OTHERstudy of socioeconomic and demographic variables
PROCEDURECAM exercise therapy
PROCEDUREpsychosocial assessment and care
PROCEDUREquality-of-life assessment
PROCEDUREstress management therapy

Timeline

Start date
2008-08-01
Primary completion
2010-04-01
Completion
2010-04-01
First posted
2009-05-18
Last updated
2015-06-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00903474. Inclusion in this directory is not an endorsement.