Mindfulness-Based Art Therapy for Cancer Patients

NCT ID: NCT00034970

Last Updated: 2006-08-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

114 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-04-30

Study Completion Date

2003-12-31

Brief Summary

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The purpose of this study is to determine whether cancer patients who receive the mindfulness-based art therapy (MBAT) program demonstrate improvement in health-related quality of life, a reduction in stress-related symptoms, and enhanced coping responses.

Detailed Description

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Psychosocial interventions, especially supportive-expressive group therapies, have been associated with significant improvements in health status, quality of life and coping behaviors, in patients with cancer. The purpose of the proposed pilot research study is to investigate a newly developed group therapy for cancer patients, MBAT. This proposed, randomized, controlled study follows a successful preliminary investigation of MBAT conducted at Thomas Jefferson University Hospital. MBAT integrates known benefits of art therapy, group therapy, and mindfulness-based stress reduction. Each of these fundamentally different modalities has documented usefulness in the treatment of cancer patients. The multi-modal approach is designed to enhance both the supportive and expressive aspects of the group experience. The study will be done with 96 patients who have a variety of cancer types. Participants will be matched for age and assigned randomly to either the MBAT experimental group or a non-intervention control group. Both groups will continue to receive their usual oncologic/medical care. The MBAT program consists of eight weekly meetings of two and one half-hours in length. At the end of the eight weeks, participants in the control group will be crossed over to the experimental intervention arm for an additional eight weeks. Participants will be assessed pre- and post-intervention on measures of health-related quality of life, psychological distress, and coping, using standardized outcome instruments (SF-36, SCL-90-R and COPE). Our long-term goal is to collect sufficient data to determine the overall efficacy of this promising intervention and to identify which patients are particularly likely to benefit from MBAT.

Conditions

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Cancer

Keywords

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alternative medicine art cancer combination cancer therapy creative-expression group therapy holistic human therapy evaluation meditation neoplasm /cancer chemotherapy coping gender difference outcomes research psychological aspect of cancer psychological stressor quality of life racial /ethnic difference stress management support behavioral /social science research patient oriented research

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

ECT

Blinding Strategy

NONE

Interventions

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Mindfulness-based at therapy

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of cancer or cancer recurrence within the past 2 years.
* Able to tolerate 8 weekly groups, 2 1/2 hours in length

Exclusion:

* Less than 4 months from original or recurrent diagnosis or beyond 2 years
* Physically unable to attend groups
* Non-stabilized major mental disorder
* Children
* Comprehension of written and spoken English at a level of less than 4th grade.
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Center for Complementary and Integrative Health (NCCIH)

NIH

Sponsor Role lead

Principal Investigators

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Daniel A. Monti, MD

Role: PRINCIPAL_INVESTIGATOR

Thomas Jefferson University

Caroline Peterson, MA

Role: STUDY_DIRECTOR

Thomas Jefferson University

Locations

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Thomas Jefferson University Hospital/Kimmel Cancer Center

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

References

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Reibel DK, Greeson JM, Brainard GC, Rosenzweig S. Mindfulness-based stress reduction and health-related quality of life in a heterogeneous patient population. Gen Hosp Psychiatry. 2001 Jul-Aug;23(4):183-92. doi: 10.1016/s0163-8343(01)00149-9.

Reference Type BACKGROUND
PMID: 11543844 (View on PubMed)

Speca M, Carlson LE, Goodey E, Angen M. A randomized, wait-list controlled clinical trial: the effect of a mindfulness meditation-based stress reduction program on mood and symptoms of stress in cancer outpatients. Psychosom Med. 2000 Sep-Oct;62(5):613-22. doi: 10.1097/00006842-200009000-00004.

Reference Type BACKGROUND
PMID: 11020090 (View on PubMed)

Other Identifiers

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R21AT000683-01

Identifier Type: NIH

Identifier Source: org_study_id

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