ClinConnect ClinConnect Logo
Search / Trial NCT06419647

Tracking Mood: The Effects of Daily Mood Tracking VAS on Alcohol Consumption in Adult Heavy Drinkers

Launched by ILONA MYLLYNIEMI · May 13, 2024

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Alcohol Aud Mood Tracking Ema Emotional Monitoring Alcohol Tracking

ClinConnect Summary

This clinical trial, called "Tracking Mood," is studying how keeping track of one's mood might affect how much alcohol people drink. Specifically, it's looking at adults in the UK who drink heavily—more than 20 units of alcohol per week. Participants in the study will be divided into two groups. One group will track their mood every day using a simple scale, while the other group will just report how much time they spend online. The researchers believe that by regularly tracking moods, participants may be able to reduce their alcohol consumption, which could help improve their overall health.

To be eligible for this study, participants need to be over 18 years old, speak fluent English, and drink more than 20 units of alcohol each week. They should also be located in the UK and have a good track record of completing previous studies on the Prolific platform. However, individuals with ongoing mental health conditions are not eligible to participate. The study will take place entirely online, making it convenient for those who qualify.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Speaking fluent English
  • being over 18 years of age
  • High completion rates of previous studies on the Prolific platform
  • Being located in the United Kingdom
  • Consuming over 20 UK units of alcohol per week
  • Exclusion Criteria:
  • Having an ongoing mental health condition

About Ilona Myllyniemi

Ilona Myllyniemi is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative studies. With a focus on rigorous scientific methodology and ethical standards, Myllyniemi oversees a diverse portfolio of clinical trials that span various therapeutic areas. Her expertise in trial design, regulatory compliance, and stakeholder engagement ensures that each study is conducted with the highest level of integrity and efficacy. By fostering collaboration among researchers, healthcare professionals, and participants, Ilona Myllyniemi plays a pivotal role in driving the development of new treatment options and contributing to the advancement of medical science.

Locations

Patients applied

0 patients applied

Trial Officials

Valerie Voon, PhD, MD

Study Director

University of Cambridge

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported