NCT06981702

Brief Summary

The aimed this study is to determine the effect of regular exercise program on mood, chronotype and sleep quality in university students.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 13, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

May 21, 2025

Completed
28 days until next milestone

Study Start

First participant enrolled

June 18, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 18, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 26, 2025

Completed
Last Updated

October 2, 2025

Status Verified

May 1, 2025

Enrollment Period

1 month

First QC Date

May 13, 2025

Last Update Submit

September 30, 2025

Conditions

Keywords

physical activitydepressionchronotype

Outcome Measures

Primary Outcomes (3)

  • Pittsburgh Sleep Quality Index

    This index includes 19 items designed to evaluate sleep quality in the last month. Subjective sleep quality consists of sleep latency, sleep duration, habitual sleep efficiency, sleep disturbance, sleeping pill use and daytime sleep dysfunction. Each component is evaluated on a 0-3 scale. The total score has a value between 0-21. A high total score indicates poor sleep quality. A total PSQI score greater than 5 is an indicator of a significant level of sleep disturbance. The validity and reliability studies of this scale for our country were conducted by Ağargün et al. in 1996.

    immediately after application

  • Morningness-Eveningness Questionnaire - MEQ

    This scale helps determine when individuals are more active and awake in accordance with their biological clocks. The scale consists of a total of 19 items and includes questions aimed at determining whether individuals are morning type, evening type, or intermediate type. These questions cover topics such as individuals' sleep and wakefulness habits, performance levels in the morning and evening hours, and when they feel more energetic. The sum of the scores given to each item determines the person's morning or evening tendency: Morning individuals are more energetic in the early hours and work more efficiently in the morning. Evening individuals are more energetic in the late hours and work more efficiently in the evening. Intermediate individuals, on the other hand, can perform in a balanced manner at different times of the day without showing a clear morning or evening tendency. The total score helps classify the individual as being in accordance with their circadian rhythm. The v

    immediately after application

  • Beck Depression Inventory- BDI

    This scale is widely used in the evaluation of depression, especially in psychiatric practices and clinical research. The BDI consists of a total of 21 items, and each item includes the basic symptoms of depression (e.g. sadness, hopelessness, sleep disorders, appetite changes, feelings of worthlessness). Each item is scored between 0 and 3. Scores increase according to the severity of the individual's symptoms, and the total score varies between 0 and 63. Individuals who score between 0 and 13 have no or mild depression. Scores between 14 and 28 indicate moderate depression. Scores between 29 and 63 indicate severe depression. A high total score indicates more severe depression. The BDI is frequently used to better understand individuals' depression levels and to monitor progress in the treatment process. The validity and reliability studies of this scale were conducted by Hisli in 1986.

    immediately after application

Study Arms (1)

Study Group

ACTIVE COMPARATOR

. In our study, demographic information (age, gender, height, weight, education, marital status, occupation, where and with whom they live), additional diseases, medications used, whether they live in a rural or urban area, whether they have had any sleep problems before, and whether they have had any psychiatric diagnoses before will be recorded for all subjects. Before the exercise, students will fill out the Pittsburgh Sleep Quality Index to determine their sleep quality, the Morningness-Eveningness Scale to assess their chronotype, and the Beck Depression Inventory to measure their depressive symptom levels, and the results will be recorded. Students taking the body mechanics course will be asked to do aerobic exercises they learned in class, three days a week, including warm-up and cool-down, for a total of 60 minutes of exercise. The exercises will be performed on the same days and times each week. All exercises performed by the students for 8 weeks will be monitored by the rese

Other: Exercise

Interventions

. In our study, demographic information (age, gender, height, weight, education, marital status, occupation, where and with whom they live), additional diseases, medications used, whether they live in a rural or urban area, whether they have had any sleep problems before, and whether they have had any psychiatric diagnoses before will be recorded for all subjects. Before the exercise, students will fill out the Pittsburgh Sleep Quality Index to determine their sleep quality, the Morningness-Eveningness Scale to assess their chronotype, and the Beck Depression Inventory to measure their depressive symptom levels, and the results will be recorded. Students taking the body mechanics course will be asked to do aerobic exercises they learned in class, three days a week, including warm-up and cool-down, for a total of 60 minutes of exercise. The exercises will be performed on the same days and times each week. All exercises performed by the students for 8 weeks will be monitored by the resea

Study Group

Eligibility Criteria

Age18 Years - 49 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Studying at Aydın Adnan Menderes University Söke Health Services College,
  • Taking the body mechanics course,
  • Being between the ages of 18-49,
  • Being able to read, speak and understand Turkish.

You may not qualify if:

  • Having received physical therapy services due to musculoskeletal diseases in the last 3 months,
  • Having musculoskeletal diseases such as ankylosing spondylitis, chronic or structural joint diseases,
  • Having congenital malpositions of the musculoskeletal system,
  • Having a physical disability,
  • Having undergone artificial joint replacement,
  • Having multiple sclerosis, myodystrophic or other neurodegenerative diseases, Having serious diseases such as acute herniated disc, Using muscle relaxants or other drugs that affect muscle elasticity, Having a cardiovascular disease, Having a history of previous back surgery, Having a traffic accident in the last 6 months, Not being within the age range determined for the study, Having a mental disability that prevents answering the comprehension and evaluation forms.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aydin Adnan Menderes University

Aydin, Turkey (Türkiye)

Location

MeSH Terms

Conditions

DepressionAnxiety DisordersMotor Activity

Interventions

Exercise

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorMental Disorders

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Şenay Demir Yazıcı

    Aydin Adnan Menderes University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 13, 2025

First Posted

May 21, 2025

Study Start

June 18, 2025

Primary Completion

July 18, 2025

Study Completion

September 26, 2025

Last Updated

October 2, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations