Psychotherapy (Accelerated Resolution Therapy) for Cancer Related Trauma and Distress
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- STATUS
- Recruiting
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- participants needed
- 30
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- sponsor
- Mayo Clinic
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.
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. We 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 randomized controlled trial (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.
Details
Condition | Hematologic Malignancy, hematologic neoplasms, Metastatic Malignant Neoplasm, hematologic neoplasms, Malignant Solid Neoplasm |
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Age | 18years - 100years |
Treatment | Questionnaire Administration, Psychotherapy |
Clinical Study Identifier | NCT04436835 |
Sponsor | Mayo Clinic |
Last Modified on | 16 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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