A Mixed Methods Evaluation of HPI Resilience Intervention Study

Completed · Not applicable

Conditions studied: Stress

In brief

The primary objective of the Resilience Study is to determine the impact of the Corporate Athlete® Resilience product through recalibrating mindset and changing resilience supportive behavior. Analysis will be performed via Survey and Study Interviews (two methods) to determine how the CAR Training recalibrated and impacted the Research Participants mindset and resilience state. 1\. Tool: Stress Mindset Measure-General (SMM-G) Additional analysis will evaluate participants' engagement in behavior changes in the first 30 days. 2\. Tool: Energy Management Behaviors. Secondary objectives include further analysis to determine if the intervention group demonstrated significant improvements in the following measures: 1\. Brief Resilience Scale (BRS) 2\. Public Health Surveillance Wellbeing (PHS-WB) 3\. Sleep Habits (Rand MOS) 4\. Health, Wellbeing and Productivity (SF36, HPQ) 5\. Work Productivity and Activity Impairment (WPAI) 6\. Brief Cope 7\. Perceived Stress (PSS) In addition, demographic assessments will be collected.

Key facts

Study ID

NCT03451240

Run by

Johnson & Johnson Health and Wellness Solutions, Inc.

People needed

30

Starts

2017-09-16

Expected to finish

2017-12-31

Last updated by the study team

2018-03-01

Who can join

Age: 18 and older, up to 110. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Be an adult (18 years or older);
• Be a participant in the LNLP (i.e., provided consent for the project);
• Meet =>2 stress experience level parameters on Stress Mindset Measure-General (SMM-G);
• Meet =< 4.3 on the Brief Resilience Scale (BRS);
• Be willing to attend a full day training program at the Lake Nona Institute during the designated training date;
• Be willing to provide email and phone number as a contact method;
• Must speak, read, and understand English fluently;
• Be able to comprehend and follow the requirements of the study;
• Research Participant must have a valid e-mail address;
• Be able to provide Informed Consent;
• Be willing and able to comply with all study procedures for the duration of the study.

You may not qualify if…

• Is not an adult (18 years or older);
• Has not consented to participate in the LNLP;
• Does not meet the stress or resilience parameters (as defined above);
• Unwilling or unable to provide consent and sign the ICF;
• Unwilling or unable to complete study related questionnaires;
• Have a physical or cognitive impairment that would interfere with their ability to provide accurate information;
• Not able to speak, read, or understand English fluently.

Where it is running

• The Human Performance Institute — Orlando, Florida, United States

Full record on ClinicalTrials.gov

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