ClinicalTrials.gg
Not yet recruitingNCT07867743Updated Oct 9, 2026

Effects of a Classroom-Integrated Exercise Program on Neck Health and Performance in Dental Students

An interventional study of Exercise program in Neck Disability, sponsored by Giresun University. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Giresun University · Not applicable, Interventional, and Other

Updated Oct 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
64
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This non-randomized controlled intervention study aims to evaluate the effects of a six-week structured exercise program integrated into anatomy laboratory sessions on neck pain, neck-related disability, musculoskeletal symptoms, physical performance, and laboratory performance among first- and second-year dental students at Giresun University.

Second-year students will constitute the intervention group, while first-year students will serve as controls and continue their routine educational activities. The intervention consists of five-minute exercise sessions performed twice weekly before anatomy laboratory classes for six weeks. Assessments will be conducted at baseline and at the end of the intervention, with additional assessments of neck pain and disability at week three and six.

Read the detailed description

Musculoskeletal symptoms, particularly neck-related complaints, are common among dental students and may begin during the early stages of professional training. Prolonged static posture, neck flexion, and ergonomically unfavorable positions during educational and laboratory activities may contribute to the development of these symptoms. Integrating brief preventive exercises into routine educational activities may therefore provide a feasible approach to promoting musculoskeletal health without requiring additional sessions outside the curriculum.

This study is a non-randomized, controlled, pretest-posttest intervention study conducted among first- and second-year dental students at Giresun University. Individual randomization is not feasible because anatomy laboratory sessions are conducted with each academic year attending as a whole group. Therefore, second-year students constitute the intervention group and first-year students constitute the control group.

The intervention consists of a structured six-week exercise program integrated into anatomy laboratory sessions. The program is designed to include brief exercises targeting cervical mobility and strength, posture, and scapular musculature. The control group continues its routine educational activities without receiving the exercise intervention during the study period.

Participants are evaluated before and after the intervention using self-reported and objective measures addressing neck health, musculoskeletal symptoms, and physical performance. Selected neck-related outcomes are also assessed during the intervention period. Laboratory performance and participants' responses to the exercise program are monitored during the study period. The overall aim is to determine whether a brief exercise program that can be incorporated into routine anatomy laboratory education has beneficial effects on neck health and related functional and physical outcomes in dental students.

02

Conditions studied

  • Neck Disability

Keywords

  • Neck disability
  • dental students
  • physical performance
03

In context

Lead sponsor

Giresun University is the lead sponsor of 57 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being a first- or second-year dental student at Giresun University.
  • Being older than 18 years.
  • Providing voluntary

Exclusion criteria

Exclusion Criteria:

  • Diagnosed cervical disc herniation
  • Rheumatological disease
  • History of neck trauma
  • Receiving regular physiotherapy
  • Chronic neurological disease
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
64 participants (estimated)

Study arms

  • Experimental
    Intervention arm: Exercise Intervention Group

    Intervention arm: Second-year dental students will participate in a six-week structured exercise program integrated into anatomy laboratory sessions.

    Behavioral: Exercise program

  • No intervention
    Control arm: Control Group

    First-year dental students will continue their routine anatomy laboratory education without receiving the exercise intervention.

Interventions

  • BehavioralExercise program

    The intervention consists of a six-week structured exercise program performed twice weekly before anatomy laboratory sessions. Each session lasts approximately five minutes and includes breathing exercises, cervical mobility exercises, isometric cervical strengthening, postural exercises, and scapular strengthening. The first two weeks are supervised by a researcher, followed by video-guided sessions for the remaining four weeks. No exercise equipment is required.

06

What researchers measure

Primary outcomes

  1. neck disability index

    Neck-related disability will be assessed using the Neck Disability Index (NDI), a 10-item self-reported questionnaire. Each item is scored from 0 to 5, resulting in a total score ranging from 0 to 50. Higher scores indicate greater neck-related disability.

    Time frame: Baseline, week 3, and week 6

  2. Change in Cervical and Shoulder Muscle Strength

    Muscle strength will be assessed isometrically using a handheld dynamometer. Cervical flexion, extension, lateral flexion, and shoulder external rotation strength will be measured in the sitting position. Each measurement will be performed three times, with at least 30 seconds of rest between measurements, and the highest value will be recorded. Higher values indicate greater muscle strength.

    Time frame: Baseline and 6 weeks

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2026; primary completion for Nov 2026, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 5, 2026
First posted
Oct 9, 2026
StartEst.
Oct 8, 2026
Primary completionEst.
Nov 27, 2026
CompletionEst.
Feb 28, 2027
Last update
Oct 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07867743
Lead sponsor
Giresun University
Responsible party
Asuman Okur (Assistant Professor, Giresun University) — Principal investigator
First posted
Oct 9, 2026
Start date
Oct 8, 2026 (estimated)
Primary completion
Nov 27, 2026 (estimated)
Completion
Feb 28, 2027 (estimated)
Last update
Oct 9, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion