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Not yet recruitingNCT07525414CORE-DENT TriaUpdated Apr 13, 2026

Core Stability and Hand Function in Dental Students

An interventional study of Core Stability Exercise Program in Core Stability, Hand Grip Strength and Manual Dexterity, sponsored by Burdur Mehmet Akif Ersoy University. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by Burdur Mehmet Akif Ersoy University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to evaluate whether a core stability exercise program can improve core endurance, hand grip strength, pinch strength, and manual dexterity in dental students. The study will include adult dental students who are enrolled at a university and do not have any musculoskeletal or neurological conditions.

The main questions it aims to answer are:

Does a 6-week core stability exercise program improve core endurance in dental students? Does the exercise program improve hand grip strength, pinch strength, and manual dexterity compared to usual daily activities?

Researchers will compare a core stability exercise group to a control group to determine whether the exercise program is more effective than routine daily activities.

Participants will:

Be randomly assigned to either an exercise group or a control group Participate in a supervised core stability exercise program three times per week for 6 weeks (exercise group only) Continue their usual daily activities without additional exercise (control group) Undergo assessments of core endurance, hand grip strength, pinch strength, and manual dexterity before and after the intervention period

02

Conditions studied

  • Core Stability
  • Hand Grip Strength
  • Manual Dexterity
  • Dental Students

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Keywords

  • Core Stability
  • Hand Function
  • Manual Dexterity
  • Dental Students
  • Exercise
03

In context

Motor Activity

9,798 studies on the registry are indexed under Motor Activity; 1,910 are open to participants now.

This study's planned enrollment of 44 is below the median of 60 across 8,388 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Burdur Mehmet Akif Ersoy University is the lead sponsor of 48 studies on the registry; 17 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

  • Students enrolled in the Faculty of Dentistry at Burdur Mehmet Akif Ersoy University
  • Aged 18 years or older
  • Right-hand dominant
  • No diagnosed musculoskeletal, chronic systemic, or neurological disorder
  • No regular exercise habits
  • Able to understand and follow study instructions
  • Able to speak and understand Turkish
  • Willing to participate voluntarily and provide informed consen

Exclusion criteria

Exclusion Criteria:

  • History of spinal or upper extremity injury or surgery
  • Presence of disc pathology or cervical spine disorders
  • Severe pain affecting upper extremity function
  • Any acute injury occurring during the study period that may affect performance
  • Inability to complete assessments
  • Withdrawal from the study for any reason
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    Core Stability Exercise Group

    Participants in this group will receive a supervised core stability exercise program for 6 weeks, performed three times per week. Each session will last approximately 30-45 minutes, including warm-up, core stabilization exercises, and cool-down phases. All sessions will be conducted under the supervision of a physiotherapist.

    Behavioral: Core Stability Exercise Program

  • No intervention
    Control Group

    Participants in this group will not receive any structured exercise program and will be instructed to continue their usual daily activities. They will be asked not to initiate any new exercise programs during the study period.

Interventions

  • BehavioralCore Stability Exercise Program

    A structured and progressive core stability exercise program will be conducted over 6 weeks, with three supervised sessions per week. Each session will last 30-45 minutes and include warm-up, core stabilization exercises, and cool-down. The program consists of three progressive phases: Weeks 1-2 focus on core activation and static exercises on a stable surface (e.g., abdominal draw-in, bridge, plank); Weeks 3-4 include dynamic exercises on a stable surface (e.g., bird-dog, curl-up, superman); Weeks 5-6 involve resistance and unstable surface training (e.g., Swiss ball exercises, rotational movements, resisted exercises). All sessions will be supervised by a physiotherapist. Exercise intensity and progression will be individualized based on participant performance, and safety will be monitored throughout.

06

What researchers measure

Primary outcomes

  1. Core Endurance

    Core endurance will be assessed using the McGill core endurance test battery, including trunk flexor endurance, trunk extensor endurance, and side bridge tests. The duration (in seconds) that participants can maintain each position will be recorded.

    Time frame: Baseline and after 6 weeks

Secondary outcomes

  1. Hand Grip Strength

    Hand grip strength will be measured using a hydraulic hand dynamometer. Three measurements will be taken for each participant, and the average value will be used for analysis.

    Time frame: Baseline and after 6 weeks

  2. Pinch Strength

    Pinch strength will be measured using a pinch meter, including tip-to-tip, lateral (key pinch), and palmar (three-point pinch) grip types. Three measurements will be taken and averaged.

    Time frame: Baseline and after 6 weeks

  3. Manual Dexterity

    Manual dexterity will be assessed using the Purdue Pegboard Test, including dominant hand, non-dominant hand, both hands, and assembly tasks. Scores will be recorded as the number of items completed within specified time periods.

    Time frame: Baseline and after 6 weeks

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Abd-Elfattah HM, Aly SM. Effect of Core Stability Exercises on Hand Functions in Children With Hemiplegic Cerebral Palsy. Ann Rehabil Med. 2021 Feb;45(1):71-78. doi: 10.5535/arm.20124. Epub 2021 Feb 9. PubMed 33557483 ↗
  • Suzer A, Buker N, Gungor HR, Ok N, Savkin R. Effects of telerehabilitation-implemented core stability exercises on patient-reported and performance-based outcomes in total knee arthroplasty patients: randomised controlled trial. Physiother Theory Pract. 2025 Jun;41(6):1213-1227. doi: 10.1080/09593985.2024.2411312. Epub 2024 Oct 7. PubMed 39374044 ↗
  • Jeffreys, Ian MSc, CSCS. Developing a Progressive Core Stability Program. Strength and Conditioning Journal 24(5):p 65-66, October 2002.
  • Jha P, Nuhmani S, Kapoor G, Al Muslem WH, Joseph R, Kachanathu SJ, Alsaadi SM. Efficacy of core stability training on upper extremity performance in collegiate athletes. J Musculoskelet Neuronal Interact. 2022 Dec 1;22(4):498-503. PubMed 36458387 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Apr 2026; primary completion for Feb 2027, 10 months later.

Of 5,147 non-industry interventional studies with no phase under Motor Activity, half reached primary completion within 17 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 36. This study's planned 10 months is below that.

Counting every sponsor, half of 5,207 studies reached it within 17 months; a quarter within 7 and three quarters within 36.

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

Registered
Apr 6, 2026
First posted
Apr 13, 2026
StartEst.
Apr 2026
Primary completionEst.
Feb 2027
CompletionEst.
Jun 2027
Last update
Apr 13, 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.
No changes since tracking began. The registry record was last updated on Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07525414
Lead sponsor
Burdur Mehmet Akif Ersoy University
Responsible party
Akın Süzer (PT, PhD, Assistant Professor, Burdur Mehmet Akif Ersoy University) — Principal investigator
First posted
Apr 13, 2026
Start date
Apr 2026 (estimated)
Primary completion
Feb 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
Apr 13, 2026

Study contacts

Akın Süzer, PT, PhD
Contact
akinsuzer@mehmetakif.edu.tr
+90 555 484 3024

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 Apr 2026. You cannot join it, but the record below documents what was studied.

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