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NCT04560595 · ClinicalTrials.gov registry record · NA

Remote Guided Caffeine Reduction

A NA study, sponsored by Johns Hopkins University.

Completed
Registry status
NA
Development phase
109
Enrollment target

NCT04560595: Completed NA study, sponsored by Johns Hopkins University.

NCT04560595 is a NA study that has completed, run by Johns Hopkins University. The registered enrollment target is 109 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT04560595, a NA study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
NA
Development phase
109 participants
Enrollment target

Study Summary

The purpose of this online research study is to determine whether or not a gradual caffeine reduction program developed at Johns Hopkins can help people reduce their caffeine use. The investigators will provide materials to help guide caffeine reduction and ask questions to track caffeine use over several weeks. The investigators will also assess how reducing caffeine may benefit common caffeine-related problems such as anxiety, sleep disturbances, and gastrointestinal distress. The study will also determine whether or not people like participating in this caffeine reduction program in an online format.

Primary Outcome

To determine to what extent participants will engage with a remote caffeine reduction intervention for caffeine-related problems and find it acceptable, we will calculate the percentage of completed assessments for each video visit among eligible participants.

Interventions

  • BEHAVIORAL Caffeine Reduction Manual

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2020-09-10
Est. Completion 2023-10-01
Phase NA
Johns Hopkins University

1,448 total trials

What the finished NCT04560595 record still lists

NCT04560595 is an interventional study that assigns participants to a tested intervention. The registered 109 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Caffeine Reduction Manual is the first listed.

NCT04560595 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04560595 about?

NCT04560595 is a clinical study titled "Remote Guided Caffeine Reduction". The purpose of this online research study is to determine whether or not a gradual caffeine reduction program developed at Johns Hopkins can help people reduce their caffeine use. The investigators will provide materials to help guide caffeine reduction and ask questions to track caffeine use over s...

What is the current status of trial NCT04560595?

This trial is currently completed. It is a NA study. The enrollment target is 109 participants. The study started on 2020-09-10. Estimated completion is 2023-10-01.

What interventions are being tested in trial NCT04560595?

The interventions under investigation include: Caffeine Reduction Manual (BEHAVIORAL).

Who is sponsoring clinical trial NCT04560595?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04560595's enrollment target sits among peer trials

109 825th of 2000 higher than 1,176 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04560595, the US trial registry maintained by the National Library of Medicine. NCT04560595 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.