A Pilot Study of a Brief Pre-Operative Intervention for Patients Undergoing Breast Surgery
NCT ID: NCT02939040
Last Updated: 2017-10-06
Study Results
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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COMPLETED
NA
22 participants
INTERVENTIONAL
2016-06-30
2017-02-28
Brief Summary
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Detailed Description
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Intervention Procedures - The Positive Piggy Bank. Participants randomized to this group will first get an overview of the intervention, learn about the rationale for this treatment, and receive supplies including the instructions on a decorative card, a piggy bank, and paper currency slips (pieces of lined paper with a place for the date). Participants in this group will be instructed to do the activities as detailed above in the Positive Piggy Bank instructions daily until the evening before surgery (approximately 21 days). On the evening before surgery, they are to "close their account" by opening the piggy bank and reviewing all of the slips of paper.
Study personnel will contact patients within 72 hours of beginning the study to answer questions and/or provide encouragement. Participants will also be contacted on the day before surgery to let them know that they should read all of their currency slips and reminded to bring their currency slips with them to the hospital on the day of surgery.
On the day of surgery, prior to surgery they will complete the first set of follow-up questionnaires. They will also be reminded that these same follow-up questionnaires will be administered by phone 14 days after surgery.
The control group will serve to show the relative benefits of the Positive Piggy Bank intervention. These participants will follow the same questionnaire completion procedures as listed above including phone calls. The phone call at 72 hours will be to simply thank them for their participation in the study.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Positive Activities Intervention
Patients will note at least one positive event each day, write it down on a slip of paper and then deposit this piece of paper in a piggy bank. After approximately 21 days, the participant reads each one the night before surgery.
Positive Activities
The PPB intervention involves noting at least one positive event each day, writing it down on a slip of paper and then depositing this piece of paper in a piggy bank. This practice is to take place at the end of the day, every day over a circumscribed period of time. At the end of the "deposit period" the participant "closes the account" and makes a full withdrawal by taking all of the slips out of the piggy bank and reading each one the night before surgery.
Usual Care Group
The control group will serve to show the relative benefits of the Positive Piggy Bank intervention. These participants will follow the same questionnaire completion procedures.
No interventions assigned to this group
Interventions
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Positive Activities
The PPB intervention involves noting at least one positive event each day, writing it down on a slip of paper and then depositing this piece of paper in a piggy bank. This practice is to take place at the end of the day, every day over a circumscribed period of time. At the end of the "deposit period" the participant "closes the account" and makes a full withdrawal by taking all of the slips out of the piggy bank and reading each one the night before surgery.
Eligibility Criteria
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Inclusion Criteria
2. Ages 18 and above.
3. Able to read/understand English and give consent.
4. Willing and able to comply with all aspects of study procedures.
5. No plan to initiate a new program that could affect well-being during the study period (e.g., psychotherapy, new exercise regimen, meditation classes).
Exclusion Criteria
2. Having a psychotic disorder or the presence of another psychiatric condition (e.g., severe depression \[i.e., score on the PHQ-9\], suicidal ideation) or cognitive impairment (e.g., severe dyslexia, traumatic brain injury) limiting ability to give consent and/or participate fully in the study.
3. Other factors that at the discretion of the investigators would adversely affect study.
18 Years
FEMALE
No
Sponsors
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University of Michigan
OTHER
Responsible Party
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Afton Hassett, Psy.D.
Associate Research Scientist
Principal Investigators
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Afton Hassett, Psy.D.
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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University of Michigan, Chronic Pain and Fatigue Research Center
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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UMCC 2016.036
Identifier Type: OTHER
Identifier Source: secondary_id
HUM00114087
Identifier Type: -
Identifier Source: org_study_id