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Clinical Trials in Ireland / NCT07422727
Enrolling by invitation Not applicable

Impact of Cooling Mats on Vasomotor Symptoms in Patients Receiving Endocrine Therapy

NCT07422727 · tracked via the Priya Life Science Ireland tracker
Sponsor
Sligo General Hospital
Phase
Not applicable
Started
2025-11-10
Last updated
2026-02-20

Condition(s) studied

Hot FlashesSleepHormonalCancer

Investigational drug(s) / intervention(s)

Cooling Gel Mats

Cooling Gel Mats: Participant will use the Cooling gel mats for 8 weeks at night

Study summary

This research study will investigate whether using a non-drug option, like a cooling mat, made of temperature-regulating materials, can help relieve the discomfort of hot flushes and/or night sweats for people receiving hormone treatment following a cancer diagnosis.

Cooling mats are made from specialised material designed to keep body temperature in a comfortable range by reducing heat. Previous research has shown these materials can be helpful for managing hot flushes during menopause, and the investigators are investigating if the same benefits apply to cancer patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: Age ≥ 18 years at time of consent Histologically confirmed diagnosis of breast cancer or prostate cancer Currently receiving endocrine therapy (e.g., tamoxifen, aromatase inhibitors, ovarian suppression therapy, androgen deprivation therapy) Self-reported vasomotor symptoms (e.g., hot flushes and/or night sweats) occurring at least once daily during the 2 weeks prior to screening Ability to understand the study procedures and provide written informed consent Exclusion Criteria: Prior use of cooling mat devices specifically for management of vasomotor symptoms within the past 3 months Known hypersensitivity or allergy to polyvinyl chloride (PVC) or any component of the cooling mat device Cognitive impairment, psychiatric condition, or other medical condition that, in the opinion of the investigator, would interfere with adherence to study procedures Concurrent participation in another interventional clinical trial for management of vasomotor symptoms

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
SligoUniversity HospitaL Sligo Sligo

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07422727 on ClinicalTrials.gov ↗ ← All trials in Ireland