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RecruitingNCT07329400Updated Jan 13, 2026

Turkish Adaptation and Validation of the Burnt Hand Outcome Tool (BHOT)

An observational study in Hand Burn, Hand Injuries and Burn Injuries, sponsored by Necmettin Erbakan University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-13.

Sponsored by Necmettin Erbakan University · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Nov 2025; still recruiting 10 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this observational study is to evaluate the validity and reliability of the Turkish adaptation of the Burnt Hand Outcome Tool (BHOT) in adults with a history of hand burns. The participant population will include adults aged 18 years and older who have experienced unilateral or bilateral hand burns and can read and understand Turkish.The main questions this study aims to answer are:

Does the Turkish version of the BHOT demonstrate high internal consistency, test-retest reliability, and construct validity? How strongly are BHOT scores associated with objective hand function measures such as grip strength and sensory evaluation? Participants will not be assigned to comparison groups, as this is a methodological validation study.

Participants will: Complete a sociodemographic information form. Complete the Turkish version of the BHOT and the QuickDASH questionnaire. Undergo objective assessments including hand grip strength using a dynamometer and sensory evaluation using Semmes-Weinstein monofilaments. Participate in repeated assessments at baseline, 1 month, 3 months and 6 months for reliability analyses.

02

Conditions studied

  • Hand Burn
  • Hand Injuries
  • Burn Injuries

Keywords

  • Hand Burns
  • Burnt Hand Outcome Tool (BHOT)
  • Validation Study
  • Reproducibility of Results
  • Burn Injuries
03

In context

Hand Injuries

108 studies on the registry are indexed under Hand Injuries; 31 are open to participants now.

This study's planned enrollment of 100 is above the median of 73 across 20 observational studies indexed under Hand Injuries.

Browse Hand Injuries studies →

Lead sponsor

Necmettin Erbakan University is the lead sponsor of 198 studies on the registry; 48 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
No
Sampling method
Non-probability sample

Study population

Adult patients aged 18 years and older with a history of second-degree or higher burn injury in one or both hands who are receiving outpatient or inpatient care at the burn unit. All participants are able to read and understand Turkish and provide informed consent.

Inclusion criteria

  • Age 18 years or older
  • History of second-degree or higher burn injury in one or both hands
  • Ability to read and understand Turkish
  • Willingness to participate and provision of written informed consent

Exclusion criteria

Exclusion Criteria:

  • History of trauma, surgery, or rheumatologic disease affecting hand function prior to the burn injury
  • Age under 18 years
  • Cognitive impairment or psychiatric disorder preventing completion of the questionnaires
  • Refusal to participate or withdrawal from the study at any time
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Interventions

  • OtherBurnt Hand Outcome Tool (BHOT) - Turkish Version

    Assessment using the Turkish version of the Burnt Hand Outcome Tool (BHOT) for validity and reliability evaluation; no treatment is applied.

06

What researchers measure

Primary outcomes

  1. Reliability of the Turkish Version of the Burnt Hand Outcome Tool (BHOT)

    Total score of the Turkish version of the Burnt Hand Outcome Tool (BHOT-T), a patient-reported outcome measure assessing functional, aesthetic, sensory, and psychosocial outcomes in adults with hand burns. The BHOT-T consists of 20 items, each scored on a Likert scale. Total scores range from 0 to 80, with higher scores indicating worse outcomes / greater negative impact of hand burns on hand function and quality of life.

    Time frame: Baseline , 1 month, 3 months, and 6 months

  2. Construct Validity of Burnt Hand Outcome Tool-Turkish

    Construct validity will be assessed using confirmatory factor analysis (CFA) to evaluate the factor structure of the Turkish version of Burnt Hand Outcome Tool.

    Time frame: baseline, 1 month, 3 months, and 6 months

Secondary outcomes

  1. Convergent Validity With QuickDASH

    Total score of the Quick Disabilities of the Arm, Shoulder and Hand questionnaire (Quick DASH), a patient reported outcome measure assessing upper extremity disability. Scores are reported as units on a scale from 0 to 100, with higher scores indicating greater disability.

    Time frame: Baseline, 1 month, 3 months, and 6 months

  2. Hand Grip Strength

    Hand grip strength measured in kilograms (kg) using a hand dynamometer in adults with hand burns.

    Time frame: Baseline

  3. Sensory Function Assessment

    Sensory function of the hand assessed using the Semmes-Weinstein Monofilament Test, reported as monofilament level indicating cutaneous sensory threshold.

    Time frame: Baseline

  4. Discriminant Validity by Clinical Characteristics

    Discriminant validity will be evaluated by comparing total scores of the Turkish version of the Burnt Hand Outcome Tool (Burnt Hand Outcome Tool - Turkish version, BHOT-T) across predefined clinical subgroups, including burn severity, history of skin grafting, and working status.

    Time frame: Baseline

07

Study locations

1 of 1 sites recruiting
  • Konya City Hospital (Konya Şehir Hastanesi)
    Konya, Meram, Turkey (Türkiye)
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 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
NCT07329400
Lead sponsor
Necmettin Erbakan University
Collaborators
Konya City Hospital
Responsible party
Pariya Pouriyamanesh (MSc student in Physiotherapy and Rehabilitation, Necmettin Erbakan University) — Principal investigator
First posted
Jan 9, 2026
Start date
Nov 17, 2025
Primary completion
Apr 2026 (estimated)
Completion
Nov 2026 (estimated)
Last update
Jan 13, 2026

Study contacts

Pariya Puriyamanesh
Contact
fzt.pariya@gmail.com
+905538304970

Oversight

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

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