CClinicalTrials.gg
CompletedNCT00248911Updated Feb 23, 2017

The Effect Of Meditation On Quality Of Life In Women With Breast Cancer And Other Gynecological Cancers

An interventional study of Mindfulness based meditation program in Breast Cancers and Gynecologic Cancer, sponsored by Weill Medical College of Cornell University. Completed at 1 site in United States. Open to female participants aged 18 Years to 101 Years. Per ClinicalTrials.gov, last updated 2017-02-23.

Sponsored by Weill Medical College of Cornell University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Not applicable
Ages
18 Years to 101 Years
Sex
Female
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Study summary

Women with breast cancer and other gynecologic cancers often suffer significant distress and disability from their disease. A practice of meditation-based stress reduction and cognitive-affective-behavioral learning may help women with these conditions decrease their suffering and improve their quality of life.

Read the detailed description

The objective of this project in women recently treated for breast or other gynecologic cancer is to determine whether an intervention program consisting of group and individual instruction in a meditation-based practice of stress-reduction and cognitive-affective-behavioral learning has the potential for reducing disabling distress and improving quality of life in a population vulnerable to the progression or recurrence of disease. Quality of life will be assessed at 12 months.

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Conditions studied

  • Breast Cancers
  • Gynecologic Cancer

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Keywords

  • Breast cancer
  • Gynecologic cancers
  • Meditation
  • Stress-reduction
  • Cognitive-affective behavioral learning
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In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's enrollment of 94 is above the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Weill Medical College of Cornell University is the lead sponsor of 867 studies on the registry; 160 are open to participants now.

Of its 119 completed or terminated interventional studies of FDA-regulated products, 91 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 101 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • All women with stage I-III breast or other gynecologic cancer who have received treatment within the preceding year will be eligible for inclusion in the study.

Exclusion criteria

Exclusion Criteria:

  • Patients who refuse to participate will be excluded
  • Patients with Metastatic cancer are excluded.
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
94 participants (actual)

Study arms

  • Experimental
    Mindfulness based meditation program

    Meditation and Breast Cancer: Subjects will participate in an intervention consisting of group and individual instruction in a meditation-based practice of stress-reduction and cognitive-affective-behavioral learning.

    Behavioral: Mindfulness based meditation program

Interventions

  • BehavioralMindfulness based meditation program

    Subjects will participate in an intervention consisting of group and individual instruction in a meditation-based practice of stress-reduction and cognitive-affective-behavioral learning.

    Also known as: Meditation and Breast Cancer

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What researchers measure

Primary outcomes

  1. Quality of life will be assessed by within patient differences in the FACT-G (General Functional Assessment of Cancer Treatment Scale), as well as with the disease specific subscales at baseline and at 12 months.

    Time frame: Subjects will complete questionnaires at baseline and closeout. Patients will participate in the meditation program weekly for 20 weeks.

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Study locations

1 site
  • Weill Cornell Medical College-New York Hospital
    New York, New York 10065, United States
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References and documents

Individual participant data

Plan to share: No — No Plan to Share IPD

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 23, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00248911
Lead sponsor
Weill Medical College of Cornell University
Collaborators
Avon Foundation
Responsible party
Mary E. Charlson, MD (Principal Investigator, Weill Medical College of Cornell University) — Principal investigator
First posted
Nov 4, 2005
Start date
May 2003
Primary completion
Mar 2010
Completion
Mar 2010
Last update
Feb 23, 2017

Study contacts

Mary E Charlson, MD
principal investigator · Weill Medical College of Cornell University
Joseph Loizzo, MD,PhD
principal investigator · Center for Complementary and Intergrative Medicine, New York Presbyterian Hospital-Weill Cornell Medical College

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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