TEMPO: Testing the Effect of Mindfulness for Prostatectomy Outcomes
Study Details
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Part 2: Couples-based mindfulness intervention Mindfulness-based intervention + Usual care |
Behavioral: Mindfulness-based Intervention
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.
Behavioral: Usual Care
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.
|
| Active Comparator: Part 2: Usual care Usual care |
Behavioral: Usual Care
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.
|
Outcome Measures
Primary Outcome Measures
- Change in level of distress assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) Anxiety [Change from baseline at 3 and 6 months post-prostatectomy]
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. [Change from baseline at 3 and 6 months post-prostatectomy]
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 [Change from baseline at 3 and 6 months post-prostatectomy]
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) [Change from baseline at 3 months post-prostatectomy]
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 [Change from baseline to 3 months post-prostatectomy]
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) [Change from baseline at 3 months post-prostatectomy]
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) [Change from baseline at 3 and 6 months post-prostatectomy]
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.
Eligibility Criteria
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
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Rogel Cancer Center | Ann Arbor | Michigan | United States | 48109 |
Sponsors and Collaborators
- University of Michigan Rogel Cancer Center
Investigators
- Principal Investigator: Lindsey Herrel, MD, MS, University of Michigan
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- UMCC 2018.129
- HUM00152158