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A Mobile App for Hot Flashes and Sleep Disturbances

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Conditions

Hot FlashesHypnosispost-menopausalmhealthappshypnotherapy

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of the study is to compare the possible efficacy and acceptability of two mobile health applications for the reduction of hot flashes and related symptoms.This study is completely remote, and participants will be be asked to engage with a mobile health application daily for five weeks and provide feedback and experience with the app.

Official Title

A Mobile App for Hot Flashes and Sleep Disturbances (Evia): Randomized Controlled Trial

Quick Facts

Study Start:2025-01-10
Study Completion:2025-08-21
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06718803

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:40 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 40 years or older and able to consent to participate in the study.
  2. * Self-reported history of a minimum of 36 hot flashes per week at baseline.
  3. * Ability to access the app to which the participant is randomized to (the Evia app or the Talli Care app).
  4. * Ability to speak and understand English. Non-English speakers are not considered in this study because the Apps are currently only offered in English.
  1. * New or changes in the current use of any prescription or complementary and alternative medicine (CAM) treatments for hot flashes during the duration of the intervention. \[If the participant is already using any prescription or CAM, they will be asked to provide details of ingredients, dose and frequency. They will be permitted to participate in the study if they agree to no change for the duration of their participation in the study and otherwise meet inclusion criteria.\]
  2. * Does not have access to a Smartphone
  3. * Severe or unstable medical or psychiatric illness.
  4. * Current use of hypnosis for any condition.

Contacts and Locations

Study Locations (Sites)

Baylor University
Waco, Texas, 76706
United States

Collaborators and Investigators

Sponsor: Baylor University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01-10
Study Completion Date2025-08-21

Study Record Updates

Study Start Date2025-01-10
Study Completion Date2025-08-21

Terms related to this study

Keywords Provided by Researchers

  • Hypnosis
  • post-menopausal
  • mhealth
  • apps
  • hypnotherapy
  • hot flashes

Additional Relevant MeSH Terms

  • Hot Flashes