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Impact of a Physical Activity Intervention on Sleep Quality, Mental and Physical Well-Being in Health Sciences Students

U

University of Sfax

Status

Not yet enrolling

Conditions

Well-being
Physical Activity
Sleep Quality
Sedentary Lifestlye

Treatments

Behavioral: Weekend Warrior Physical Activity Program
Behavioral: Regular Weekly Physical Activity Program

Study type

Interventional

Funder types

Other

Identifiers

NCT07140185
FMS110590-80-25

Details and patient eligibility

About

This randomized controlled trial aims to compare the effects of a regular weekly physical activity program versus a "Weekend Warrior" activity pattern on sleep quality, physical well-being, and mental well-being in sedentary university students. Participants will be randomly assigned to one of the intervention groups or to a control group and assessed at baseline and after the intervention.

Full description

Sedentary behavior is a growing concern among university students and is associated with poor sleep quality, fatigue, and lower mental well-being. Physical activity interventions can improve these outcomes, but the optimal frequency and pattern of activity remain unclear. This randomized controlled trial will evaluate and compare the effects of a regular weekly physical activity schedule with those of a "Weekend Warrior" pattern, in which the recommended amount of exercise is concentrated in two sessions per week. Sedentary university students will be randomly assigned to one of two intervention groups or to a control group for an 8-10 week period. Sleep quality (measured by actigraphy), physical well-being, and mental well-being will be assessed before and after the intervention. The findings of this study may help to inform public health recommendations for physical activity patterns among young adults.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged 18 to 25 years.
  • Low level of physical activity, determined using the validated International Physical Activity Questionnaire (IPAQ) according to its scoring thresholds.
  • Provided written informed consent.
  • Available to participate in the entire intervention program and all planned assessments.

Exclusion criteria

  • Current use of medications that may affect sleep quality or alertness (e.g., sedative hypnotics, sedative antidepressants, psychostimulants).
  • History of serious medical conditions or any contraindication to moderate physical activity.
  • Morbid obesity.
  • Current pregnancy during the study period.
  • Participation in another intervention program simultaneously.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 3 patient groups

Arm 1 - Regular Weekly Physical Activity
Experimental group
Description:
Participants in this group will engage in structured physical activity sessions three times per week, each lasting 50 minutes, over a period of 8 weeks. The sessions include a combination of aerobic exercises, supervised by trained instructors. The goal is to distribute the recommended weekly activity evenly across the week.
Treatment:
Behavioral: Regular Weekly Physical Activity Program
Arm 2 - Weekend Warrior Physical Activity
Experimental group
Description:
Participants in this group will perform the same total weekly physical activity as Arm 1, but concentrated in 2 sessions during the weekend. Each session lasts approximately 75 minutes and includes aerobic exercises, supervised by the same trained instructors.
Treatment:
Behavioral: Weekend Warrior Physical Activity Program
Arm 3 - Control / No Intervention
No Intervention group
Description:
Participants in this group will maintain their usual lifestyle without any structured physical activity intervention during the study period. After study completion, they may be offered the Regular Weekly physical activity program.

Trial contacts and locations

1

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Central trial contact

Soumaya CHAABENE, PhD student; Soumaya CHAABENE, PhD student

Data sourced from clinicaltrials.gov

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