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
1 other identifier
interventional
140
1 country
1
Brief Summary
This study will consist of an experimental group and a control group. Approximately 150 adult males and females from the ages of 19+ will take part in this study. Subjects will be divided into a Control and Experimental Group. Subjects for the control and experimental group will be recruited from our internal database of subjects who have previously shown interest in studies and from userinterviews. Subjects in the experimental group (RPM Group) will be admitted to the Tony Robbins Rapid Planning Method (RPM) virtually at no cost, while the 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. 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable anxiety
Started Aug 2024
Shorter than P25 for not_applicable anxiety
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 2, 2024
CompletedFirst Posted
Study publicly available on registry
August 6, 2024
CompletedStudy Start
First participant enrolled
August 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2024
CompletedSeptember 16, 2025
September 1, 2025
2 months
August 2, 2024
September 10, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Purpose in life test
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).
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Work Extrinsic and Intrinsic Motivation Scale (WEIMS)
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.
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Life and productivity test
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.
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Secondary Outcomes (2)
PERMA Profiler
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Rosenberg's Self esteem scale
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Other Outcomes (2)
Generalize Anxiety Disorder (GAD-7)
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Perceived Stress Scale (PSS-10)
Pre - Event, 1 week Post - Event, 1 Month Post - Event
Study Arms (2)
Experimental
EXPERIMENTALSubjects 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.
Control
ACTIVE COMPARATORSubjects 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.
Interventions
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Applied Science and Performance Institute
Tampa, Florida, 33634, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 2, 2024
First Posted
August 6, 2024
Study Start
August 20, 2024
Primary Completion
November 1, 2024
Study Completion
November 1, 2024
Last Updated
September 16, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared