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Performance & Recovery Protocols

A 12-item assessment examining sideline recovery practices, treatment barriers, and technology readiness across collegiate and professional athletic programs.

Informed Consent & Data Use

Sponsor. This survey is conducted by Temp°IQ™, a thermoregulation technology company operating under ISO 13485 quality management and FDA regulatory oversight.

Purpose. The purpose of this survey is to assess current practices, unmet needs, and technology readiness within your professional domain. Responses directly inform Temp°IQ™ product development, clinical research priorities, and regulatory strategy.

Voluntary Participation. Your participation is entirely voluntary. You may decline to answer any question or withdraw at any time by closing this page. Your decision to participate or withdraw will not affect any professional relationship with Temp°IQ™.

Confidentiality & Anonymization. All responses are anonymized and reported only in aggregate. Individual responses are never shared with third parties. Contact information, if optionally provided, is stored separately from survey data and used only for the purposes described below.

Data Use & Retention. De-identified response data may be used to support product design, regulatory submissions (including FDA filings), and peer-reviewed publications. Data will be retained for a minimum of five (5) years in accordance with FDA record retention requirements.

Data Platform. This survey is administered via REDCap (Research Electronic Data Capture), a secure, HIPAA-compliant web-based platform designed for clinical research data collection and hosted within a SOC 2 Type II certified environment.

Estimated Time. 4–6 minutes (12 items).

Contact. For questions about this survey or your rights as a participant, contact the Temp°IQ™ research team at study@tempiq.com.

Section A — Respondent Profile

Question 1 of 12

Which best describes your primary role?

Question 2 of 12

At what competitive level do you primarily work or compete?

Question 3 of 12

Approximately how many athletes do you support or treat per season?

Section B — Current Recovery & Thermal Practice

Question 4 of 12

What is your primary method of acute thermal intervention on the sideline or in the training room?

Question 5 of 12

How satisfied are you with your current recovery program's ability to manage both the physical and psychological aspects of injury?

Very Dissatisfied Very Satisfied

Question 6 of 12

To what extent does your current protocol allow athletes to remain engaged with their team during treatment?

Not at All Completely

Section C — Barriers & Unmet Needs

Question 7 of 12

Which barriers limit the effectiveness of your current recovery program? Select all that apply.

Question 8 of 12

Which body regions require thermal intervention most frequently in your practice? Select all that apply.

Section D — Technology Readiness

Question 9 of 12

How likely are you to adopt a wearable, programmable thermal device that allows athletes to train or compete during treatment?

Very Unlikely Very Likely

Question 10 of 12

Which device capabilities would most influence your adoption? Select up to three.

Question 11 of 12

How important is peer-reviewed evidence in your decision to adopt a new recovery technology?

Not Important Essential

Section E — Open Response

Question 12 of 12

What single advancement in recovery technology would most improve outcomes for your athletes?

Optional — Stay Connected

Providing your contact information is entirely voluntary. It will be stored separately from your survey responses and used only to share study results or product updates.

Disclaimer. This survey is for research and product development purposes only. It does not constitute medical advice, clinical diagnosis, or a professional consultation. Temp°IQ™ assumes no liability for decisions made based on participation in this survey. Responses are provided at the participant’s own discretion.

Survey data is captured via REDCap, a secure platform developed at Vanderbilt University and used by over 6,400 institutions worldwide for clinical and translational research.

Thank You

Your responses have been recorded and will be reviewed by our research team. Aggregated findings may be published in future Temp°IQ™ technical reports.

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