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NCT06539949 · ClinicalTrials.gov registry record · NA
Efficacy of the Tony Robbins Rapid Planning Method (RPM)
A NA study of Anxiety and Stress, sponsored by Applied Science & Performance Institute.
- Completed
- Registry status
- NA
- Development phase
- 140
- Enrollment target
- 1
- Study location
NCT06539949: Completed NA study of Anxiety and Stress, sponsored by Applied Science & Performance Institute.
NCT06539949 is a NA study of Anxiety and Stress that has completed, run by Applied Science & Performance Institute. The registered enrollment target is 140 participants, below the 440-participant average among 364 other Anxiety trials with a reported enrollment target (68% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06539949, a NA study of Anxiety and Stress, has completed, sponsored by Applied Science & Performance Institute.
- COMPLETED
- Registry status
- NA
- Development phase
- 140 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
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
Conditions Studied
Interventions
- BEHAVIORAL Rapid Planning Method (RPM)
- BEHAVIORAL Journaling
Study Locations (1)
Florida
- The Applied Science and Performance Institute - Tampa
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 140 participants |
| Start Date | 2024-08-20 |
| Est. Completion | 2024-11-01 |
| Phase | NA |
What the finished NCT06539949 record still lists
NCT06539949 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, below the 440-participant average among 364 other Anxiety trials with a reported enrollment target (68% lower).
The record links to 6 conditions, with Anxiety appearing as the primary indexed condition, and to 2 interventions - of which Rapid Planning Method (RPM) is the first listed.
NCT06539949 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT06539949 about?
NCT06539949 is a clinical study titled "Efficacy of the Tony Robbins Rapid Planning Method (RPM)". 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 ou...
What is the current status of trial NCT06539949?
This trial is currently completed. It is a NA study. The enrollment target is 140 participants. The study started on 2024-08-20. Estimated completion is 2024-11-01.
What conditions does trial NCT06539949 study?
This clinical trial studies the following conditions: Anxiety, Stress, Mood, Well-Being, Psychological, Motivation.
What interventions are being tested in trial NCT06539949?
The interventions under investigation include: Rapid Planning Method (RPM) (BEHAVIORAL), Journaling (BEHAVIORAL).
Who is sponsoring clinical trial NCT06539949?
This trial is sponsored by Applied Science & Performance Institute, which has 20 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06539949 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06539949's enrollment target sits among peer trials
140 129th of 364 higher than 235 of 364 other Anxiety trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Anxiety trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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