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NCT Number: NCT07372105

Validation of the French Version of the SERQoL Questionnaire

This observational study aims to validate the French version of the Smile Esthetics-Related Quality of Life (SERQoL) questionnaire in adult patients recruited in two APH-HP dental departments. The study evaluates internal consistency, test-retest reliability, and construct validity of the questionnary. A total of 120 patients will be recruited from dental departments at two AP-HP hospitals.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

This psychometric validation study involves adult patients receiving their first consultation at AP-HP dental services. The SERQoL questionnaire will be completed twice (at baseline and after 15 days). Internal consistency (Cronbach's alpha), test-retest reliability (intraclass or Pearson correlation), and factor structure (confirmatory factor analysis) will be analyzed. No clinical intervention is involved, and participation will not alter standard care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Patients attending their first periodontal consultation at the oral medicine departments of Rothschild Hospital (AP-HP) or Charles Foix Hospital (AP-HP)
  • Patients who speak and understand French well enough to read and understand the study information sheet.
  • Patients who are informed and do not object to participating in the study

Exclusion criteria

  • Patients under guardianship or curatorship
  • Patients who are completely edentulous, whether the edentulism is compensated or not
  • Patients with multiple dental agenesis (more than 6 teeth), amelogenesis, or syndromic or non-syndromic dentinogenesis imperfecta
  • Patients with psychiatric illnesses that may impact body image, such as patients with anorexia-bulimia or body dysmorphic disorder.

Treatment and study plan

Primary outcomes

  1. Measure of the internal consistency by the Cronbach's alpha

    Time frame: Day 15

    Measure of the questionnaire internal consistency by the Cronbach's alpha

  2. Measure of the test-retest reliability by the intraclass or Pearson correlation

    Time frame: Day 15

    Measure of the questionnaire test-retest reliability by the intraclass or Pearson correlation

  3. Measure of the factor structure by the confirmatory factor analysis.

    Time frame: Day 15

    Measure of the questionnaire factor structure by the confirmatory factor analysis

Secondary outcomes

  1. Average score measure by gender

    Time frame: Day 0

    Average questionnaire score measure by gender

  2. Average score measure by age

    Time frame: Day 0

    Average questionnaire score measure by gender

  3. Average score measure according to periodontal health status

    Time frame: Day 0

    Average questionnaire score measure according to periodontal health status

Study contacts

Contact information is provided by the study sponsor or research team.

Bruno TAVERNIER, PU-PH

CONTACT

[email protected]

+33 (0)1 40 19 39 85

Suzanne DIMPRE, CCU-AAH

CONTACT

[email protected]

00 33 1 40 19 39 85

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Validation of the French Version of the Smile Esthetics-Related Quality of Life (SERQoL) Questionnaire

Acronym: Periosmile1

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 28, 2026
Registry last updated
Jan 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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