Acceptance and Commitment Therapy for Chronic Pain in Cancer Survivors



Status:Recruiting
Conditions:Chronic Pain, Chronic Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:18 - 100
Updated:12/21/2018
Start Date:December 4, 2018
End Date:January 2023
Contact:Ashley Pratt-Cordova
Email:ashley.pratt-cordova@ucdenver.edu
Phone:720-848-5521

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A study to help manage chronic pain in cancer survivors through Acceptance and Commitment
Therapy (ACT) after undergoing active cancer treatment, such as surgery, chemotherapy, and/or
radiation.

This study attempts to apply effective pain management interventions from other chronic pain
populations to those of cancer related populations. It will assess the ability of ACT to
alleviate chronic cancer related pain and evaluate ease of implementation of treatment.
Patients will be allocated to either the intervention group (ACT) or the control group,
getting them the usual course of treatment.

Inclusion Criteria:

1. Provision to sign and date the consent form

2. Stated willingness to comply with all study procedures and be available for the
duration of the study

3. Be a male or female aged 18-100

4. Have pathology confirmed diagnosis of a solid tumor cancer

5. Be three or more months out from active cancer treatment (surgery, chemotherapy,
and/or radiation)

6. Endorses experiencing pain for three or more months prior to eligibility screening

7. Indicates moderate to severe difficulties with pain interference as related to their
cancer experience, with a score of 4 or higher on the pain interference item from the
Chronic Pain Grading Questionnaire

8. Shows no evidence of cancer disease (NED) or with stable, chronic disease under
"watchful waiting"

9. Fluent in English

10. Psychiatric stability as assessed by chart review and study personnel (e.g., not
exhibiting symptoms consistent with diagnoses of serious mental illness such as active
psychosis or mania)

Exclusion Criteria:

1. Having pain that can be solely attributed to a diagnosis outside of their cancer
experience

2. Presenting with barriers to group participation (e.g., social anxiety) or when
group-based provision of care would impede participant's treatment or that of other
group members

3. Patients with a diagnosis of malignant neoplasm of the brain (ICD-10 C71) or malignant
neoplasm of spinal cord, cranial nerves and other parts of central nervous system
(ICD-10 C72).
We found this trial at
1
site
12605 East 16th Avenue
Aurora, Colorado 80045
720-848-0000
Principal Investigator: Emily Cox-Martin, PhD
Phone: 720-848-5521
University of Colorado Hospital, Site Top medical professionals, superior medicine and progressive change make University...
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