- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06539949
Efficacy of the Tony Robbins Rapid Planning Method (RPM)
Investigation of Efficacy of the Tony Robbins Rapid Planning Method (RPM) on Life Productivity and Mood States - a Controlled Experimental Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
For the journaling control group, subjects will be asked to write a weekly to-do-list at least once weekly at the beginning of the week. And at least read, or refer to their journal on a daily basis as direction for the work activities of the day.
The 3-day RPM (Rapid Planning Method) event by Tony Robbins involves online seminar based training sessions designed to enhance participants' productivity, goal-setting abilities, and time management skills. On the first day, subjects engage in virtual workshops focused on establishing clear, specific, and achievable goals through the RPM framework, which emphasizes purpose-driven planning. Day two consists of interactive virtual sessions where participants develop personalized action plans, incorporating Robbins' strategies for prioritizing and organizing tasks. Throughout the event, participants partake in motivational exercises aimed at increasing engagement, self-efficacy, and clarity of vision. The final day includes collaborative virtual activities where subjects practice RPM techniques in real-world scenarios, receive feedback, and refine their plans.
Psychological assessment surveys will be taken before the event, and at 1 week (day 8-13), and 4 weeks (day 29-34) post intervention. The control group will take the psychological assessment before beginning journaling, and at 1 week (day 8-13), and 4 weeks (day 29-34) post intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Florida
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Tampa, Florida, United States, 33634
- The Applied Science and Performance Institute
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Ages 19+
- Male and Female
- English literate
- Willing to sign the study informed consent form
- Experimental group: must participant in Tony Robbins Rapid Planning Method (RPM)
- Control group: must be willing to journal regularly
Exclusion Criteria:
- Excluded from the experimental group if you DO NOT participate in RPM
- Excluded from the control group if you DO participate in RPM, or any other Tony Robbins sponsored event during the study intervention
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: Control
Subjects assigned to the control group, will not attend the event, but instead be required to regularly complete journaling involving a to-do-list of their weekly work tasks.
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Subjects will be keeping a weekly to-do list.
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Experimental: Experimental
Subjects in the experimental group (RPM Group) will be admitted to the Tony Robbins Rapid Planning Method (RPM) virtually at no cost.
RPM™ , developed by Tony Robbins, is a new system of thinking that is purported to help you align your daily actions with your life's purpose.
During RPM, Tony will coach participants how to implement these life strategies.
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RPM is a three day immersive seminar.
Subjects will be exposed to a variety of mind-body exercises and psycho educational content including neural linguistic programming, designed to motivate, inspire, and improve the quality of people's lives.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Purpose in life test
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
|
The PIL test is a 20-item self-report attitudinal scale designed to measure the extent to which a respondent perceives a general sense of meaning and purpose in life or respectively suffers from an "existential vacuum".
This test is the first and the most-studied questionnaire to measure perceived life purpose and meaning.
It consists of 11 items which focus on the respondents' mood (e.g., item 1: I am usually completely bored, neutral, exuberant, enthusiastic), 3 items which address life goals (e.g., item 3: In life I have no goals or aims at all, neutral, very clear goals and aims), and 3 items which address meaning of life itself (e.g., item 4: My personal existence is utterly meaningless without purpose, neutral, very purposeful and meaningful).
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
|
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Work Extrinsic and Intrinsic Motivation Scale (WEIMS)
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
|
is divided into three-item six subscales, which correspond to the six types of motivation (i.e., intrinsic motivation, integrated, identified, introjected and external regulations, and motivation).
Participants will be asked to indicate on a Likert-type scale ranging from 1 (does not correspond at all) to 7 (corresponds exactly) the extent to which the items represent the reasons they are presently involved in their work.
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
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Life and productivity test
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
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these are 30 Likert scale questionnaires, measured on a scale of 1 to 10, with 1 meaning "strongly disagree", and 10 meaning "strongly agree".
It consists of 5 items which focus on the respondents productivity, 3 items which focus on time management skills, 4 items which focus on emotions, 14 items which focus on engagement, and 4 items which focus on clarity of vision and purpose.
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PERMA Profiler
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
|
The scale measures five aspects of well-being defined by Martin Seligman, PERMA - positive emotion, engagement, relationships, meaning, and accomplishment, as well as negative emotion and health.
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
|
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Rosenberg's Self esteem scale
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
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A 10-item scale that measures global self-worth by measuring both positive and negative feelings about the self.
The scale is believed to be uni-dimensional.
All items are answered using a 4-point Likert scale format ranging from strongly agree to strongly disagree.
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Generalize Anxiety Disorder (GAD-7)
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
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a self report-based survey that assesses generalized anxiety disorder and severity on a 7-item scale.
Scores of 5, 10, and 15 are taken as the cut-off points for mild, moderate and severe anxiety, respectively.
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
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Perceived Stress Scale (PSS-10)
Time Frame: Pre - Event, 1 week Post - Event, 1 Month Post - Event
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measures global perceived stress via self-report on a ten item scale.
Scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress.
Total scores ranging from 0-13 would be considered low stress.
Total scores ranging from 14-26 would be considered moderate stress.
Total scores ranging from 27-40 would be considered high perceived stress.
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Pre - Event, 1 week Post - Event, 1 Month Post - Event
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pro00081040
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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