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Clinical Trials/NCT04436835
NCT04436835
Completed
Not Applicable

Accelerated Resolution Therapy for Cancer Related Trauma and Distress: a Pilot Study

Mayo Clinic1 site in 1 country21 target enrollmentNovember 27, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hematopoietic and Lymphoid System Neoplasm
Sponsor
Mayo Clinic
Enrollment
21
Locations
1
Primary Endpoint
Cancer distress
Status
Completed
Last Updated
last year

Overview

Brief Summary

This trial studies whether a form of psychotherapy called accelerated resolution therapy can help with cancer distress and psychological trauma. Accelerated resolution therapy is an evidence-based therapy for the treatment of depressive symptoms, trauma, and stress-related disorders. This study may provide evidence to support integration of accelerated resolution therapy into psychological treatment of cancer patients, which may decrease cancer related trauma and distress.

Detailed Description

PRIMARY OBJECTIVES: I. Calculate changes, and estimate mean changes, in primary outcomes of psychological trauma and cancer distress over a six week time period while receiving weekly accelerated resolution therapy (ART). II. Calculate changes, and estimate mean changes, in secondary outcomes of anxiety and depression over a six week period while receiving weekly ART. III. Will use a qualitative, descriptive design to explore contextual elements of the cancer experience that are consistently distressing and/or psychologically traumatic to more fully inform a future RCT testing in ART in cancer distress and psychological trauma. IV. Calculate changes, and estimate mean changes, in secondary outcomes of resilience and symptom distress over a six week period while receiving weekly ART. OUTLINE: Patients undergo ART over 60-90 minutes once a week for up to 5 sessions. After completion of study intervention, patients are followed up at 1 week and again at 1 month.

Registry
clinicaltrials.gov
Start Date
November 27, 2019
End Date
August 19, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Cindy Tofthagen

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Able to read, write and understand English
  • Undergone chemotherapy, radiation therapy, chimeric antigen receptor T cells (CAR-T), or bone marrow transplant for a cancer diagnosis within the previous 3 years or have metastatic cancer
  • A mean score of at least 1.1 on the Cancer and Treatment Distress (CTxD) or at least one item rated at a 3 (often true) or 4 (nearly all the time)
  • A minimum score of 3 on the Primary Care-Post Traumatic Stress Disorder Screen (PC-PTSD-5)
  • Denial of suicidal ideation or intent, with no evidence of psychotic behavior
  • Participants must be willing and able to utilize secure web conferencing software, phone calls, or to travel to Mayo Clinic outside of normally scheduled visits to participate in the study

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Cancer distress

Time Frame: Up to 6 weeks

Cancer distress will be measured with the Cancer Treatment Distress Scale (CTxD). The CTxD is a 22 item Likert type scale that contains 6 subscales: uncertainty, health burden, identity, medical demands, finances, and family strain. Scores on individual items range from 0 (none) to 3 (severe) distress related to an aspect of the cancer experience.

Psychological trauma

Time Frame: Up to 6 weeks

Symptoms of psychological trauma will be measured with both the Primary Care-Post Traumatic Stress Disorder Screening (PC-PTSD-5) and the Post Traumatic Stress Disorder Checklist (PCL-5). The PCL-5 (PTSD Patient Checklist) is a 20-item self-report instrument that will be used to assess the DSM-5 symptoms of PTSD (psychological trauma). The total symptom severity score ranges from 0 to 80.

Secondary Outcomes

  • Anxiety(Up to 6 weeks)
  • Depression(Up to 6 weeks)
  • Symptom distress(Up to 6 weeks)
  • Resilience(Up to 6 weeks)

Study Sites (1)

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