NCT07520929

Brief Summary

The goal of this clinical trial is to examine the effect of a single 40-minute sauna session on glucose control in individuals at risk for metabolic impairments. Research Questions:

  • Can a single sauna session completed before a meal reduce the post-meal blood glucose response?
  • Can a single sauna session improve 24-hour glucose control? Study Design: Participants will complete two lab visits: one involving a sauna session and one placebo visit (resting condition). Researchers will compare the effects on glucose control using a continuous glucose monitor (CGM). What Participants Will Do: Attend a sauna familiarization session Have a CGM sensor placed on the upper arm Visit the lab twice (once for sauna, once for placebo) Consume three standardized meals at home after each session

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
9mo left

Started Dec 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress49%
Dec 2025Apr 2027

Study Start

First participant enrolled

December 1, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 2, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 9, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2026

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 15, 2027

Last Updated

April 9, 2026

Status Verified

April 1, 2026

Enrollment Period

1 year

First QC Date

April 2, 2026

Last Update Submit

April 2, 2026

Conditions

Keywords

saunaheat-therapyobesityoverweightcontinuous glucose monitoring

Outcome Measures

Primary Outcomes (1)

  • Incremental 2-hour postprandial glucose area under the curve (Breakfast)

    2-hour postprandial incremental AUC of CGM glucose above baseline, measured after the standardized breakfast consumed 45 minutes following the sauna or resting (control) session.

    2 hours

Secondary Outcomes (11)

  • 2-hour postprandial glucose area under the curve (Breakfast)

    2 hours

  • Incremental 2-hour postprandial glucose area under the curve (Lunch)

    2 hours

  • Incremental 2-hour postprandial glucose area under the curve (Dinner)

    2 hours

  • Incremental 2-hour postprandial glucose area under the curve (Bedtime snack)

    2 hours

  • Average incremental 2-hour postprandial glucose area under the curve (4 meals)

    2 hours

  • +6 more secondary outcomes

Study Arms (2)

Sauna

EXPERIMENTAL

Infrared sauna session

Other: Infrared sauna session

Resting control

PLACEBO COMPARATOR

Seated resting session

Other: Resting condition

Interventions

Infrared sauna session (approximately 165°F; two 20-minute sessions separated by a 5-minute rest outside the sauna)

Sauna

Seated resting session (45 minutes outside the sauna)

Resting control

Eligibility Criteria

Age30 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Are 30-55 years old
  • Have a body mass index of ≥ 27 kg/m2
  • Have a waist size \>102 cm (men) or \>88 cm (women)
  • Have access to transportation for the 2 experimental visits (e.g., car, public transit, or drop-off).
  • Are cleared for participation based on the Physical Activity Readiness Questionnaire (PAR-Q+).

You may not qualify if:

  • Take medications that affect blood sugar
  • Exercise intensely 2+ times/week
  • Have diabetes, heart issues, low blood sugar or pressure
  • Are pregnant
  • Regularly use saunas or other heat therapy 1+ times/week

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Prince Edward Island

Charlottetown, Prince Edward Island, C1A 4P3, Canada

RECRUITING

MeSH Terms

Conditions

ObesityOverweightHyperthermia

Condition Hierarchy (Ancestors)

OvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsBody Temperature ChangesHeat Stress DisordersWounds and Injuries

Study Officials

  • Etienne Myette-Cote

    University of Prince Edward Island

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Etienne Myette-Cote, PhD

CONTACT

Romina Babazadeh, MSc

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: Randomized controlled trial (pilot study)
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 2, 2026

First Posted

April 9, 2026

Study Start

December 1, 2025

Primary Completion (Estimated)

December 15, 2026

Study Completion (Estimated)

April 15, 2027

Last Updated

April 9, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations