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NCT01799733 · ClinicalTrials.gov registry record · NA

Alternative Treatments for Premenstrual Dysphoric Disorder

A NA study, sponsored by University of California, San Diego.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT01799733: Completed NA study, sponsored by University of California, San Diego.

NCT01799733 is a NA study that has completed, run by University of California, San Diego. The registered enrollment target is 43 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01799733, a NA study, has completed, sponsored by University of California, San Diego.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

The primary aim of this study is to examine the effects of co-administered wake therapy followed by light treatment on mood, and secondarily on circadian rhythms, to test the hypothesis that critically-timed chronotherapy improves mood by correcting phase disturbances in melatonin and sleep in women with Premenstrual Dysphoric Disorder.

Primary Outcome

Mood ratings include Hamilton Rating Scale for Depression (HRSD), Beck Depression Inventory (BDI), atypical depression symptoms as part of the Structured Interview Guide for the Hamilton Depression Rating Scale, Seasonal Affective Disorders version (SIGH-SAD), Beck Anxiety Inventory (BAI), mania ratings, the Psychological General Well-Being Index (PGWI) and daily mood self-ratings (DMR) that include core PMDD symptoms of anxiety and irritability as required during diagnostic evaluation, before,

Interventions

  • OTHER LWT+AM BWL
  • OTHER EWT+PM BWL

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2013-06-18
Est. Completion 2018-07-03
Phase NA
University of California, San Diego

775 total trials

What the finished NCT01799733 record still lists

NCT01799733 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which LWT+AM BWL is the first listed.

NCT01799733 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01799733 about?

NCT01799733 is a clinical study titled "Alternative Treatments for Premenstrual Dysphoric Disorder". The primary aim of this study is to examine the effects of co-administered wake therapy followed by light treatment on mood, and secondarily on circadian rhythms, to test the hypothesis that critically-timed chronotherapy improves mood by correcting phase disturbances in melatonin and sleep in women...

What is the current status of trial NCT01799733?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2013-06-18. Estimated completion is 2018-07-03.

What interventions are being tested in trial NCT01799733?

The interventions under investigation include: LWT+AM BWL (OTHER), EWT+PM BWL (OTHER).

Who is sponsoring clinical trial NCT01799733?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01799733's enrollment target sits among peer trials

43 1435th of 2000 higher than 565 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 NCT01799733, the US trial registry maintained by the National Library of Medicine. NCT01799733 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.