The impact of 4-week high-intensity interval training on mental health and sleep quality in female college students with normal weight obesity: a randomized controlled trial
Question
Does a 4-week high-intensity interval training program improve depression, anxiety, and sleep quality in female college students with normal weight obesity compared with health education/no training?
Summary
Female college students with normal weight obesity who completed a 4-week supervised bodyweight HIIT program improved depression, anxiety, and sleep-quality questionnaire scores compared with a health-education control group. The HIIT sessions were frequent, five times per week, and included 40-second bodyweight exercises with 20-second rests. The study was short, all participants were young women from one university, and adverse events were monitored generally but not reported in detail.
Methodology
- Female college students with normal weight obesity.
- 35 participants.
- Opening/closing jumps, squats, push-ups, bent-knee raises, step jumps, abdominal rolls, hip bridges, burpees, lunge squats.
- Work intervals: 40 s.
- Recovery: 20 s.
- Intensity: >90% VO2max target.
- About 34 min.
- 5 sessions/week.
- 4 weeks.
- Randomized controlled trial with pre/post assessment.
- Depression symptoms, Anxiety symptoms, and Sleep quality were tracked.
Outcomes
PHQ-9 depression score
HIIT reduced PHQ-9 while control did not change.
HIIT 5.8 +/- 4.2 to 3.2 +/- 2.7; time x group F=7.180, p=0.011; adjusted p=0.005.
GAD-7 anxiety score
HIIT reduced GAD-7 while control did not change.
HIIT 5.1 +/- 5.3 to 2.8 +/- 2.9; time x group F=8.333, p=0.007; adjusted p=0.014.
PSQI sleep quality
HIIT improved PSQI score while control did not.
HIIT 5.1 +/- 3.4 to 3.5 +/- 2.5; time x group F=11.692, p=0.002; adjusted p=0.007.
Insights
- A 40/20 bodyweight format is easy to translate into guided workouts.
- Frequent HIIT may support self-reported sleep and mood in a narrow young-adult group.
- The evidence is not sufficient to make clinical mental-health treatment claims.
Limitations
- Small sample.
- Short 4-week intervention.
- Self-report outcomes.
- No long-term follow-up.
- Unclear intensity and attendance fidelity.
Safety
- Professional coaches supervised sessions.
- Trained personnel monitored participants in real time.
- No specific adverse events were reported.