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Testing the Effect of Mindfulness for Prostatectomy Outcomes (TEMPO)

Primary Purpose

Prostate Cancer

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindfulness-based Intervention
Usual Care
Sponsored by
University of Michigan Rogel Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Cancer focused on measuring Mindfulness

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Part 2--Pilot study:

Inclusion Criteria

  • Patients aged 35 - 90 who are planning to undergo radical prostatectomy at University of Michigan Hospital
  • Partners of these men, aged 18 and older

Exclusion Criteria:

  • Participants cannot be less than 18 years of age

Sites / Locations

  • University of Rogel Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Part 2: Couples-based mindfulness intervention

Part 2: Usual care

Arm Description

Mindfulness-based intervention + Usual care

Usual care

Outcomes

Primary Outcome Measures

Change in level of distress assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) Anxiety
This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Anxiety is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of anxiety.
Change in level of distress assessed using the PROMIS SF Depression.
This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Depression is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of depression.
Change in level of distress assessed using the PROMIS SF Positive Affect and Well Being
This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Positive Affect and Well Being is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of positive affect and well being.

Secondary Outcome Measures

Change in salivary cortisol level (only patients will complete this, not partners)
Saliva is collected through an at home collection kit that is mailed to the lab.
Change in level of distress assessed using the National Comprehensive Cancer Network (NCCN) Distress Thermometer
The NCCN Distress Thermometer is a 1-item global screener of distress using a 0-10 scale with 10 being most distressed.
Change in level of distress assessed using the 5-facet Mindfulness Questionnaire (FFMQ)
FFMQ is a 15 item self-reported assessment of mindfulness. Each item is scored 1-5, with higher scores indicating higher use of 5 key facets of mindfulness: Observing; Describing; Acting with awareness; Non-judging; Non-reactivity.
Change in urinary and sexual function assessed using Michigan Urological Surgery Improvement Collaborative (MUSIC) Expanded Prostate Cancer Index Composite (EPIC-26)
MUSIC's EPIC-26 is a 26-item survey. Response options form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing higher levels of continence and better erectile function.

Full Information

First Posted
January 22, 2021
Last Updated
October 6, 2022
Sponsor
University of Michigan Rogel Cancer Center
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1. Study Identification

Unique Protocol Identification Number
NCT04727710
Brief Title
Testing the Effect of Mindfulness for Prostatectomy Outcomes
Acronym
TEMPO
Official Title
Testing the Effect of Mindfulness for Prostatectomy Outcomes (TEMPO)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Terminated
Why Stopped
Study was held due to COVID19 and unable to enroll in virtual platform
Study Start Date
August 26, 2020 (Actual)
Primary Completion Date
August 26, 2020 (Actual)
Study Completion Date
August 26, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Michigan Rogel Cancer Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This research project has 2 parts: The first part of the research is to develop a couples-based group mindfulness intervention for men undergoing prostatectomy, with input from patients and their partners. The second part is the trial registered here, which will pilot the researchers' mindfulness intervention, developed in part 1, and observe any reduction of distress for men undergoing prostatectomy and their partners.
Detailed Description
In part 1 of this research, researchers developed a couples-based group mindfulness intervention for men undergoing prostatectomy, with input from patients and their partners. Three patients who had previously undergone prostatectomy, and had expressed interest in participating in future research endeavors, and their partners were recruited to inform the design of the intervention. This group of six stakeholders identified the types of distress experienced by newly diagnosed prostate cancer patients and their partners, as well as their favored intervention approaches. These stakeholders do participate in the intervention or control groups in part 2 of this study. Researchers used thematic analysis to assess the type of distress identified by stakeholders as well as approaches favored by them. They mapped these themes on the available mindfulness approaches, identified in their review, to develop an intervention that best captures the concerns of prostate cancer survivors and partners. Part 2 is the pilot study. Researchers will enroll 20 more couples (men who are planning to undergo radical prostatectomy and their partners) to participate in a pilot study of the intervention. The pilot study will have 2 cohorts (groups). Half of the couples will be randomly assigned to the mindfulness intervention (intervention group) and the other half will receive the usual care (control group). All participants in the intervention and control groups in part 2 of the study will be analyzed to determine the effects and feasibility of the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Mindfulness

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Part 2: Couples-based mindfulness intervention
Arm Type
Experimental
Arm Description
Mindfulness-based intervention + Usual care
Arm Title
Part 2: Usual care
Arm Type
Active Comparator
Arm Description
Usual care
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-based Intervention
Intervention Description
A self-directed, web-based mindfulness training. Investigators recommend one module a week for 6 weeks. Each module is approximately 1 hour long and consists of didactic components as well as meditation and mindfulness exercises.
Intervention Type
Behavioral
Intervention Name(s)
Usual Care
Intervention Description
Standard pre-operative survivorship seminar, offered monthly to all patients at Michigan Medicine about to undergo prostatectomy and their partners is aimed at promoting realistic expectations of prostatectomy outcomes, typical side effects, rehabilitation and emotional adjustment.
Primary Outcome Measure Information:
Title
Change in level of distress assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) Anxiety
Description
This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Anxiety is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of anxiety.
Time Frame
Change from baseline at 3 and 6 months post-prostatectomy
Title
Change in level of distress assessed using the PROMIS SF Depression.
Description
This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Depression is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of depression.
Time Frame
Change from baseline at 3 and 6 months post-prostatectomy
Title
Change in level of distress assessed using the PROMIS SF Positive Affect and Well Being
Description
This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Positive Affect and Well Being is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of positive affect and well being.
Time Frame
Change from baseline at 3 and 6 months post-prostatectomy
Secondary Outcome Measure Information:
Title
Change in salivary cortisol level (only patients will complete this, not partners)
Description
Saliva is collected through an at home collection kit that is mailed to the lab.
Time Frame
Change from baseline at 3 months post-prostatectomy
Title
Change in level of distress assessed using the National Comprehensive Cancer Network (NCCN) Distress Thermometer
Description
The NCCN Distress Thermometer is a 1-item global screener of distress using a 0-10 scale with 10 being most distressed.
Time Frame
Change from baseline to 3 months post-prostatectomy
Title
Change in level of distress assessed using the 5-facet Mindfulness Questionnaire (FFMQ)
Description
FFMQ is a 15 item self-reported assessment of mindfulness. Each item is scored 1-5, with higher scores indicating higher use of 5 key facets of mindfulness: Observing; Describing; Acting with awareness; Non-judging; Non-reactivity.
Time Frame
Change from baseline at 3 months post-prostatectomy
Title
Change in urinary and sexual function assessed using Michigan Urological Surgery Improvement Collaborative (MUSIC) Expanded Prostate Cancer Index Composite (EPIC-26)
Description
MUSIC's EPIC-26 is a 26-item survey. Response options form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing higher levels of continence and better erectile function.
Time Frame
Change from baseline at 3 and 6 months post-prostatectomy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Part 2--Pilot study: Inclusion Criteria Patients aged 35 - 90 who are planning to undergo radical prostatectomy at University of Michigan Hospital Partners of these men, aged 18 and older Exclusion Criteria: Participants cannot be less than 18 years of age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lindsey Herrel, MD, MS
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Rogel Cancer Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Testing the Effect of Mindfulness for Prostatectomy Outcomes

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