ClinicalTrials.gg
RecruitingNCT07751718Updated Aug 7, 2026

Investigation of Pilates in Office Workers

An interventional study of Pilates Exercise and Desk Exercise in Office Workers and Pilates Exercise, sponsored by Firat University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-08-07.

Sponsored by Firat University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Aug 2025; still recruiting 1 year 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

When performing desk work, individuals adopt a relaxed posture and the most common musculoskeletal complaints among desk workers are neck pain, shoulder pain and lower back pain. Pilates is an exercise method in which muscles are exercised both statically and dynamically. This study is a randomized controlled trial in which a minimum of 30 female office workers working at Fırat University Faculty of Health Sciences will participate. After the participants are determined, they will be randomly divided into two groups. The study group will be given pilates training 2 days a week in addition to desk exercises; the control group will only be given desk exercises. Pain, posture and burnout will be assessed.

Read the detailed description

When performing desk work, individuals adopt a relaxed posture and the most common musculoskeletal complaints among desk workers are neck pain, shoulder pain and lower back pain. Environmental (prolonged static or awkward postures, repetitive movements and computer work) and physical (insufficient strength or muscular endurance and poor posture) factors contribute to the development of work-related neck pain. Pilates is an exercise method in which muscles are exercised both statically and dynamically. This method, which is used to increase muscle strength and spinal stability, also helps to increase endurance and correct posture.This study is a randomized controlled trial in which a minimum of 30 female office workers working at Fırat University Faculty of Health Sciences will participate. After the participants are determined, they will be randomly divided into two groups. The study group will be given pilates training 2 days a week in addition to desk exercises; the control group will only be given desk exercises. Pain, posture and burnout will be assessed. pain will be assessed with VAS, posture will be assessed with Modified NewYork...

02

Conditions studied

  • Office Workers
  • Pilates Exercise

Keywords

  • office workers
  • pilates exercises
03

In context

Lead sponsor

Firat University is the lead sponsor of 117 studies on the registry; 46 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Male and female individuals between the ages of 18-65 working in an office environment,
  • Be an office worker for the last 1 year
  • Those who read the information form and signed the consent form.

Exclusion criteria

Exclusion Criteria:

  • Individuals who have had an operation involving any musculoskeletal system in the last 2 months
  • Non-cooperative individuals
  • Pregnant women
  • Those with
  • People with chronic systemic diseases
  • Individuals who did not want to participate in the study voluntarily.
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.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
30 participants (estimated)

Study arms

  • Active comparator
    pilates group

    pilates exercises will be practiced

    Other: Pilates Exercise

  • Other
    Control group

    desk exercises will be practiced

    Other: Desk Exercise

Interventions

  • OtherPilates Exercise

    Pilates exercise

  • OtherDesk Exercise

    desk exercise

06

What researchers measure

Primary outcomes

  1. Visual analog scale (VAS)

    Back, neck, lower back and knee pain will be assessed according to the Visual Analog Scale (VAS). The VAS consists of a ten centimeter line and individuals are asked to rate their pain on a scale of zero to ten

    Time frame: up to 8 weeks

Secondary outcomes

  1. New york posture scale

    The general body posture of the patients will be evaluated with the New York Posture Rating Scale (NYPRS). NYPD was developed to evaluate the correct and incorrect alignment of various body parts in anatomical position. NYPD is a scale that allows the assessment of possible posture disorders that may occur in 13 body parts including head, neck, shoulders, waist and back, hips, knees and ankles through pictures. Within the scope of the study, one of the 3 options suitable for the patient from the 13 body parts is determined by the physiotherapist. The evaluation is completed by giving 5 points if the patient is in normal posture, 3 points if there is a moderate deterioration, and 1 point if there is a serious deterioration in posture. The results of the evaluation range between 13-65 points, with a high score indicating correct posture

    Time frame: up to 8 weeks

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Aug 2025 (actual). Primary completion is estimated for Aug 2026, 12 months after the start.

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

Registered
Feb 10, 2025
First posted
Aug 7, 2026
StartActual
Aug 10, 2025
Primary completionEst.
Aug 10, 2026
CompletionEst.
Aug 20, 2026
Last update
Aug 7, 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 Aug 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07751718
Lead sponsor
Firat University
Responsible party
Songül Bağlan Yentür (Head of Physiotherapy and Rehabilitation, Firat University) — Principal investigator
First posted
Aug 7, 2026
Start date
Aug 10, 2025
Primary completion
Aug 10, 2026 (estimated)
Completion
Aug 20, 2026 (estimated)
Last update
Aug 7, 2026

Study contacts

Songul Baglan Yentur
Contact
songulbaglan23@hotmail.com
+90 4242370000

Oversight

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

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