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Not yet recruitingNCT06865794QUALIPLASTUpdated Mar 17, 2025

Impact of Plastic and Aesthetic Surgery on Self-esteem

An observational study in Self Esteem, sponsored by Hospices Civils de Lyon. Not yet recruiting at 2 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-17.

Sponsored by Hospices Civils de Lyon · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,500
Ages
18 Years and older
Sex
All
01

Study summary

The primary objective of QUALIPLAST is to evaluate the impact of plastic and aesthetic surgery interventions on patients' self-esteem. While the demand for these procedures is steadily increasing worldwide, patients' motivations often extend beyond purely aesthetic concerns, encompassing significant psychological and emotional expectations. However, despite the growing popularity of these interventions, scientific literature remains limited when it comes to the systematic and long-term evaluation of their effects on patients' self-esteem and overall well-being.

The majority of existing studies focus on short-term outcomes or functional and physical aspects, often overlooking the psychological and emotional dimensions that play a crucial role in post-operative satisfaction. Furthermore, much research is limited to specific procedures, without adopting a comprehensive approach to plastic and aesthetic surgery. This lack of robust and generalisable data hinders a full understanding of how these interventions influence self-esteem across different types of surgeries and patient profiles.

QUALIPLAST stands out due to its multicentric, prospective, and large-scale nature, involving a wide range of procedures and collecting longitudinal data before the intervention, as well as at 3 and 12 months post-operatively. It will allow for the observation of self-esteem changes over time, providing a more complete and nuanced understanding of the effects of surgery.

This project relies on standardized and validated measurement tools, such as the Rosenberg Self-Esteem Scale, to ensure the reliability and comparability of the results. By addressing the current gaps in the literature, QUALIPLAST aims not only to enrich scientific knowledge in this field but also to provide valuable insights for healthcare professionals to improve patient care and tailor clinical practices based on the identified psychological needs.

02

Conditions studied

  • Self Esteem

Keywords

  • plastic surgery
  • cosmetic surgery
  • aesthetic surgery
03

In context

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,826 studies on the registry; 439 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

Patients consulting a plastic surgeon for one of the following operations :

  • Breast augmentation
  • Breast reduction
  • Breast lift
  • Facelift
  • Otoplasty
  • Rhinoplasty
  • Blepharoplasty
  • Abdominoplasty
  • Brachioplasty
  • Cruroplasty
  • Liposuction
  • Gender affirmation: breast augmentation
  • Gender affirmation: Facial feminisation
  • Gender affirmation: Thoracoplasty
  • Botox / Hyaluronic acid

Inclusion criteria

Patients consulting a plastic surgeon for one of the following operations:

  • Breast augmentation
  • Breast reduction
  • Breast lift
  • Facelift
  • Otoplasty
  • Rhinoplasty
  • Blepharoplasty
  • Abdominoplasty
  • Brachioplasty
  • Cruroplasty
  • Liposuction
  • Gender affirmation: breast augmentation
  • Gender affirmation: Facial feminisation
  • Gender affirmation: Thoracoplasty
  • Botox / Hyaluronic acid

Patients who agreed to take part in the study

Exclusion criteria

Exclusion Criteria:

  • Pregnant, parturient or breastfeeding women
  • Minors
  • Persons deprived of their liberty by a judicial or administrative decision
  • Persons receiving psychiatric care
  • Persons admitted to a healthcare or social institution for purposes other than research
  • Adults under a legal protection measure (guardianship, curators)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Breast augmentation

    Adult female patient undergoing breast augmentation for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Breast reduction

    Adult female patient undergoing breast reduction for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Mastopexy

    Adult female patient undergoing Mastopexy (Breast lift) for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Facelift

    Adult patient undergoing facelift for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Otoplasty

    Adult patient undergoing otoplasty for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Rhinoplasty

    Adult patient undergoing rhinoplasty for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Blepharoplasty

    Adult patient undergoing blepharoplasty for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Abdominoplasty

    Adult patient undergoing abdominoplasty for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Brachioplasty

    Adult patient undergoing brachioplasty for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Thigh lift

    Adult patient undergoing thigh lift for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Liposuction

    Adult patient undergoing liposuction for aesthetic reason

    Other: Questionnaire and Physical Exam

  • Gender affirmation: breast augmentation

    Adult patient undergoing breast augmentation gender affirmation surgery.

    Other: Questionnaire and Physical Exam

  • Gender affirmation: facial feminisation

    Adult patient undergoing facial feminisation gender affirmation surgery

    Other: Questionnaire and Physical Exam

  • Gender affirmation : thoracoplasty

    Adult patient undergoing thoracoplasty gender affirmation surgery

    Other: Questionnaire and Physical Exam

  • Injectables/Fillers

    Adult patient undergoing Botox or Hyaluronic acid injections for aesthetic reason

    Other: Questionnaire and Physical Exam

Interventions

  • OtherQuestionnaire and Physical Exam

    Rosenberg self-esteem scale pre-operatively, at 3 and 12 months post-op

    Also known as: Rosenberg self-esteem scale

  • OtherQuestionnaire and Physical Exam

    FACE-Q psychological sub-scale pre-operatively, at 3 and 12 months post-op

    Also known as: FACE-Q psychological sub-scale

  • OtherQuestionnaire and Physical Exam

    BREAST-Q psychological sub-scale pre-operatively, at 3 and 12 months post-op

    Also known as: BREAST-Q psychological sub-scale

  • OtherQuestionnaire and Physical Exam

    BSIQ-SF pre-operatively, at 3 and 12 months post-op

    Also known as: BSIQ-SF (short-form version of the Body Self-Image Questionnaire)

  • OtherQuestionnaire and Physical Exam

    FLZ psychological sub-scale pre-operatively, at 3 and 12 months post-op

    Also known as: FLZ (Fragen zur Lebenszufriedenheit / Questions on Life Satisfaction) psychological sub-scale

06

What researchers measure

Primary outcomes

  1. Self-esteem score assessed by the Rosenberg self-esteem scale

    Self-esteem score assessed by the Rosenberg self-esteem scale

    Time frame: Pre-operatively, at 3 and 12 months post-op

07

Study locations

2 sites
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06865794
Lead sponsor
Hospices Civils de Lyon
Responsible party
Sponsor
First posted
Mar 10, 2025
Start date
Apr 15, 2025 (estimated)
Primary completion
Oct 15, 2027 (estimated)
Completion
Oct 15, 2027 (estimated)
Last update
Mar 17, 2025

Study contacts

Hugo DESPERT
Contact
Hugo.despert@gmail.com
+33 6 41 50 23 29
Hugo Despert
principal investigator · Hospices Civils of Lyon

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 Mar 2025. You cannot join it, but the record below documents what was studied.

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