ACT: Impact of Acceptance and Commitment Therapy on Early Stage Breast Cancer

Sponsor
San Jose State University (Other)
Overall Status
Completed
CT.gov ID
NCT01164930
Collaborator
(none)
40
1
2
20
2

Study Details

Study Description

Brief Summary

The purpose of this randomized controlled trial is to evaluate the effectiveness of an empirically supported psychosocial treatment, Acceptance and Commitment Therapy, in facilitating improved quality of life, benefit-finding, and cortisol rhythm in breast cancer patients in an outpatient clinical oncology setting.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Acceptance and Commitment Therapy
N/A

Detailed Description

Previous research indicates that breast cancer patients may demonstrate disrupted diurnal cortisol rhythms compared to healthy individuals, and that these disrupted rhythms may be related to recurrence and earlier mortality in some patients. Interestingly, improvements in cortisol regulation in previous intervention studies for cancer patients have not necessarily been related to decreased distress. Rather, improvements in post-traumatic growth, benefit-finding, and meaningfulness have also accounted for improved neuroendocrine and immunological changes.

Traditional breast cancer groups, however, may not adequately address these areas because existing interventions often target the reduction of distress as the primary vehicle to improve psychosocial, quality of life, and biophysical outcomes. Acceptance and Commitment Therapy (ACT) is an empirically-supported, mindfulness-based psychological treatment that has been shown to enhance meaningful behavior change thorough increasing emotional acceptance of difficult psychological experiences such as distress, without the goal of changing or eliminating them.

The current study seeks to determine the preliminary effect of an 8-week ACT group in increasing positive life changes and corresponding increase in salivary cortisol slope in 40 distressed breast cancer patients, who will be randomly assigned to ACT or a wait list control group.

The hypotheses for the present study include:
  • Patients receiving ACT will demonstrate improvements in Quality of Life (QoL), Benefit-finding (BF), and health behavior compared to control group participants

  • ACT participants will demonstrate improvements in mean cortisol levels and cortisol reactivity compared to control group participants

  • These changes will be the result of increased mindful acceptance of cancer-related distress and meaningful behavior changes, rather than a reduction in distress.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Impact of Acceptance and Commitment Therapy on Salivary Cortisol in Breast Cancer
Study Start Date :
Jan 1, 2010
Actual Primary Completion Date :
Sep 1, 2011
Actual Study Completion Date :
Sep 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Acceptance and Commitment Therapy group

8-week ACT group

Behavioral: Acceptance and Commitment Therapy
8-week ACT group

No Intervention: Wait-list control group

Participants will be offered treatment following wait-list data collection

Outcome Measures

Primary Outcome Measures

  1. salivary cortisol [3-month follow-up]

Secondary Outcome Measures

  1. self-reported distress [3-month follow-up]

  2. self-reported quality of life [3-month follow-up]

  3. self-reported benefit-finding [3-month follow-up]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • diagnosis of stage I-III breast cancer

  • prescreen distress score above defined cutoff

  • agreement not to seek other breast cancer support services until study completion

Exclusion Criteria:
  • previous cancer

  • prior psychiatric treatment for serious mental health disorder (e.g., hospitalization or formal diagnosis of psychosis, major depressive episode, borderline mental retardation, suicidality, or current substance dependence)

  • current use of medications known to interfere with cortisol levels (e.g., dexamethasone)

  • major concurrent medical disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 San Jose State University San Jose California United States 95192

Sponsors and Collaborators

  • San Jose State University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jennifer A. Gregg, PhD, Assistant Professor, San Jose State University
ClinicalTrials.gov Identifier:
NCT01164930
Other Study ID Numbers:
  • 5R03CA144751-02
First Posted:
Jul 19, 2010
Last Update Posted:
Oct 4, 2021
Last Verified:
Sep 1, 2021
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 4, 2021