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Recruiting NCT06336590

Student Exercise and Sleep Timing Study - Part 2

No phase Interventional Sleep Mood Stress

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Morning Exercise.
Who it may be relevant to
Registry conditions: Sleep, Mood, Stress. Basic parameters: 18 years — 23 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The purpose of this study is to examine the effects of a morning exercise intervention on sleep (quality and duration), mood (positive affect, anxiety, depression, anger), stress and productivity among undergraduate students (18-23 years) evening-exercisers with poor self-reported sleep quality. Aim 1. Compared to the control condition, evening-exercisers prescribed morning exercise will exhibit improved sleep quality (increased efficiency, decreased fragmentation) and increased sleep duration. Aim 2. Compared to the control condition, evening-exercisers prescribed morning exercise will exhibit improved mood (increased positive affect, decreased depression, anxiety and anger). Aim 3. Compared to the control condition, evening-exercisers prescribed morning exercise will exhibit decreased stress and increased productivity.

Interventions

  • Behavioral Morning Exercise
    Exercise is changed from normal (6pm-11pm) exercise to morning (6am-11am) exercise.

Primary outcome measures

  • Sleep Quality [Time frame: 2 weeks]
Secondary outcome measures (3)
  • Mood [Time frame: 2 weeks]
  • Stress [Time frame: 2 weeks]
  • Productivity [Time frame: 2 weeks]

Eligibility criteria

Inclusion criteria

  • Healthy undergraduates (18-23 years)
  • Frequent evening exercisers (6pm-11pm, 3+ times per week)
  • Poor self-reported sleep quality
  • Must be willing to wear wrist actigraph 24/7 except when showering/bathing

Exclusion criteria

  • Sleep/circadian rhythm disorders
  • Medications for sleep
  • Inability to change schedule to exercise in AM
  • Inability to maintain exercise frequency over next 4 weeks

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 6 centers
  • College Avenue Gym — New Brunswick
  • Cook/Douglass Rec Center — New Brunswick
  • Rutgers Fitness Center — New Brunswick
  • Rutgers Sleep Lab — New Brunswick
  • Livingston Rec Center — Piscataway
  • Werblin Rec Center — Piscataway

Identifiers

NCT: NCT06336590 · Pro2024000249

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗