Menopause Clinical Trial
Official title:
Hot Water Therapy for the Treatment of Menopause-related Hot Flashes and Other Symptoms: a Clinical Trial
The purpose of this research is to determine whether hot water therapy (i.e. taking prolonged hot baths on multiple consecutive days) decreases hot flash symptoms and improves mood in women who are undergoing or who have underwent menopause. It is hypothesized that women who undergo hot water therapy will have reduced hot flash symptoms and improved mood. Initial tracking period: Women who volunteer to participate in this study will be asked to track the frequency and intensity of their hot flash and other menopause-related symptoms for an initial two week period. Afterwards, they will start their heat therapy program. Physiological assessments: On days 1, 7, and 13 of the heat therapy sessions, the participants will enter a climate controlled room to have their thermoregulatory responses assessed. This will consist of slowly walking on a motorized treadmill in 99.5°F (37.5°C) and 30% relative humidity conditions, for 30 min, after which the humidity in the climate chamber will be progressively increased until their core temperature begins to increase (~2 hour total time). Before and/or during these trials, core temperature, heart rate, whole-body sweat losses, thermal comfort, local sweat rate, and skin blood flow will be measured, and a 6 ml (~1 tsp) blood sample will be taken, to assess how the participants respond to the heat stress. These sessions should take less than 3 hours to complete. Hot water therapy sessions: Upon enrolling in the study, the participants will be assigned to one of two groups: water bathing at 105°F or 97°F in the lab. On days 2-6 and 8-12 of the therapy sessions, the participants will immerse themselves to a water level at the shoulders for ~30 min, followed by immersion to the hip level for ~60 min (total immersion time of 90 min). Post-intervention tracking period: after completing the heat therapy sessions, the participants will be asked to continue to take baths at home once every 4 days for 1 month. During this time, the participants will be asked to record the intensity and frequency of their hot flashes daily and other menopause-related symptoms weekly. At the end of this month the participants will be given a final exit survey, in order for them to provide the researchers information about their experience participating in the study.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | May 1, 2025 |
Est. primary completion date | May 1, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 40 Years to 80 Years |
Eligibility | Inclusion Criteria: - Self-reported menopause-related hot flashes Exclusion Criteria: - Diagnosed with a cardiovascular illness that precludes them from taking part in exercise |
Country | Name | City | State |
---|---|---|---|
United States | Hybl Sports Medicine and Performance Center | Colorado Springs | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Colorado Springs | East Carolina University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Exit questionnaire | Further questions for the participants to complete once at the end of the study in order to gain insight into their subjective experiences using heat therapy and to determine the likelihood the participants would implement this therapy in their lives. | One month post therapy | |
Primary | Greene climacteric questionnaire | This is a standard questionnaire used to quantify the intensity of 21 common menopause-related symptoms. The score for each question ranges in intensity from 0 (not at all) to 3 (extremely). | One month pre therapy through to one month post therapy | |
Primary | Daily hot flash diary | Based on industry-standard hot flash diaries, this tracks the number and intensity (where 1 is none and 10 is extreme) of hot flashes, night sweats, and mood disruptions that the participants feel. | One month pre therapy through to one month post therapy | |
Secondary | Core temperature | Measured using esophageal and rectal probes. Indicator of physiological heat acclimation status. | Day zero, six, and 12 of therapy | |
Secondary | Maximum skin wettedness | Maximum skin wettedness is a measure of how much of a person's skin surface they are able to wet through sweating. In an inactive, non-heat acclimated person, a normal skin wettedness value is approximately 70%. In an active, fully-heat acclimated person, a normal skin wettedness value is approximately 100%. Skin wettedness is determined by having a person walk at a constant speed on a treadmill in a 37.5degC climate chamber, while humidity levels are progressively increased. Maximum skin wettedness is determined from the humidity level in the climate chamber at which the participant's core temperature begins to rise. The more heat acclimated a person is, the higher the humidity will get to in the room before their core temperature rises. | Day zero, six, and 12 of therapy | |
Secondary | Blood plasma volume | Determined from venous blood draws. Indicator of physiological heat acclimation status. | Day zero, six, and 12 of therapy | |
Secondary | Sweat rate | Both whole-body using a high-precision platform scale and locally using the ventilated capsule technic. Indicator of physiological heat acclimation status. | Day zero, six, and 12 of therapy | |
Secondary | Skin blood flow | Determined using laser doppler flowmetry. Indicator of physiological heat acclimation status. | Day zero, six, and 12 of therapy | |
Secondary | Reproductive hormone levels (estrogen, progesterone, luteinizing hormone, orexin) | Determined from venous blood draws. Indicator hormonal status | Day zero, six, and 12 of therapy |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04553029 -
A Survey Evaluating Prevalence, Severity and Associated Factors in East Asian Women With Moderate-to-severe Menopause-related Vasomotor Symptoms (MR-VMS)
|
||
Completed |
NCT03672513 -
Short-term Supplementation, Bone Turnover and Antioxidant Status in Menopause
|
N/A | |
Terminated |
NCT03642119 -
Validation of an Objective Instrument to Measure Hot Flashes During Menopause
|
||
Completed |
NCT05387174 -
Nursing Intervention in Two Risk Factors of the Metabolic Syndrome and Quality of Life in the Climacteric Period
|
N/A | |
Completed |
NCT04210583 -
RF and PEMF for Treatment of Vaginal Laxity and Mons Pubis and Labia for Improvement of Skin Laxity
|
N/A | |
Completed |
NCT06057896 -
Effects of Combined Natural Molecules on Metabolic Syndrome in Menopausal Women
|
||
Completed |
NCT05617287 -
An Exploratory Investigation of Dietary Supplementation and the Effect on Common Symptoms of Perimenopause and Menopause
|
N/A | |
Recruiting |
NCT05180266 -
Therapeutic Touch and Music in The Menopausal Period
|
N/A | |
Recruiting |
NCT04043520 -
Bioenergetic Effects of Aging and Menopause (BEAM)
|
Phase 4 | |
Completed |
NCT03663075 -
Effect of Group Education and Individual Counselling on Mental Health and Quality of Life in 45-60 Year Old Women
|
N/A | |
Completed |
NCT03363997 -
Pharmacokinetics and Pharmacodynamics of 3 Dosages of Estriol After Continuous Vaginal Administration for 21 Days
|
Phase 1 | |
Not yet recruiting |
NCT04728126 -
Menopausal Symptoms and Burnout: Comparison of Occupational Health Issue Among Health Professionals in UMC Hospitals
|
||
Not yet recruiting |
NCT04724135 -
Assessment of Menopause Related Quality of Life Among Health Professionals in University Hospitals of UMC in Nur-Sultan
|
||
Completed |
NCT02274571 -
Raising Insulin Sensitivity in Post Menopause
|
Early Phase 1 | |
Completed |
NCT02430987 -
Low Sexual Desire and Metabolic Syndrome
|
N/A | |
Completed |
NCT02253173 -
Estradiol Vaginal Softgel Capsules in Treating Symptoms of Vulvar and Vaginal Atrophy in Postmenopausal Women
|
Phase 3 | |
Completed |
NCT01757340 -
Calorie Restriction With Leucine Supplementation
|
N/A | |
Recruiting |
NCT01488903 -
A Cohort Research of Genetic Susceptibility for Common Obesity in Women
|
N/A | |
Terminated |
NCT01633814 -
Hormone Replacement and Neural Cardiovascular Control in Postmenopausal Women
|
N/A | |
Completed |
NCT00599456 -
Investigation of the Usefulness of Omega 3 Vitamins in the Relief of Hot Flashes in Menopausal Women.
|
N/A |