NCT07533617

Brief Summary

The aim of this study is to evaluate the effects of chairs with different ergonomic designs on quality of life, discomfort, and pain in individuals with coccydynia (tailbone pain).

Trial Health

75
On Track

Trial Health Score

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

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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

April 10, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 16, 2026

Completed
15 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Expected
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Last Updated

April 16, 2026

Status Verified

April 1, 2026

Enrollment Period

1 month

First QC Date

April 10, 2026

Last Update Submit

April 10, 2026

Conditions

Keywords

Chair ergonomicsFoam geometryCoccydyniaPainPressure distributionSitting comfort

Outcome Measures

Primary Outcomes (2)

  • Pressure Distribution Measurement (Load Cell-Equipped Chair System)

    Assessment of sitting pressure distribution across right, left, and central regions in kilograms using a custom-designed load cell-integrated chair.

    Baseline + 1 week

  • Paris Questionnaire

    Evaluation of pain and functional status associated with coccydynia.

    Baseline + 1 week

Secondary Outcomes (2)

  • Extended Nordic Musculoskeletal Questionnaire (NMQ-E)

    Baseline + 1 week

  • EuroQol Quality of Life Scale (EQ-5D-3L)

    Baseline + 1 week

Study Arms (6)

Group 1: Chair with Foam Type A

EXPERIMENTAL

Participants will use ergonomically modified chair A with different foam properties during their working hours.

Device: Ergonomic Chair

Group 2: Chair with Foam Type B

EXPERIMENTAL

Participants will use ergonomically modified chair B with different foam properties during their working hours.

Device: Ergonomic Chair

Group 3: Chair with Foam Type C

EXPERIMENTAL

Participants will use ergonomically modified chair C with different foam properties during their working hours.

Device: Ergonomic Chair

Group 4: Chair with Foam Type D

EXPERIMENTAL

Participants will use ergonomically modified chair D with different foam properties during their working hours.

Device: Ergonomic Chair

Group 5: Chair with Foam Type E

EXPERIMENTAL

Participants will use ergonomically modified chair E with different foam properties during their working hours.

Device: Ergonomic Chair

Group 6: Chair with Foam Type F

EXPERIMENTAL

Participants will use ergonomically modified chair F with different foam properties during their working hours.

Device: Ergonomic Chair

Interventions

Participants will use ergonomically modified chairs with different foam properties during their working hours.

Group 1: Chair with Foam Type AGroup 2: Chair with Foam Type BGroup 3: Chair with Foam Type CGroup 4: Chair with Foam Type DGroup 5: Chair with Foam Type EGroup 6: Chair with Foam Type F

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged between 18 and 65 years
  • Working at a desk for at least 5-6 hours per day
  • Experiencing coccydynia (tailbone pain)
  • Able to sit independently without assistive support
  • No diagnosed spinal disorders (e.g., lumbar disc herniation)
  • Willing to use the assigned chair during working hours for 1 week
  • Able to understand and complete questionnaires
  • Provided written informed consent

You may not qualify if:

  • History of spinal surgery
  • Diagnosed spinal disorders (e.g., lumbar disc herniation, scoliosis, severe degenerative spine disease)
  • Neurological disorders affecting posture, sitting balance, or sensation
  • Severe musculoskeletal conditions (e.g., hip or pelvic disorders) that may affect sitting
  • Pregnancy
  • Inability to sit for prolonged periods
  • Use of assistive seating devices (e.g., orthopedic cushions) during the study period
  • Regular use of pain medication that may affect outcome measures

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kto Karatay University

Konya, 42030, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to six parallel groups, each receiving a different chair design with distinct foam properties.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 10, 2026

First Posted

April 16, 2026

Study Start (Estimated)

May 1, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 15, 2026

Last Updated

April 16, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared due to privacy and confidentiality considerations.

Locations