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PERCEPTION of QUALITY of LIFE in PATIENTS UNDERGOING ENDOSCOPIC VERTICAL GASTROPLASTY: a DESCRIPTIVE EXPLORATORY STUDY (SATIBAR)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Not yet enrolling

Conditions

ENDOSCOPIC VERTICAL GASTROPLASTY
Obesity
Endoscopy
Quality of Life of Patients

Treatments

Other: semi-structured interview on Microsoft Teams

Study type

Interventional

Funder types

Other

Identifiers

NCT06839677
7204 (Other Identifier)

Details and patient eligibility

About

An emerging alternative to bariatric surgery for the treatment of obesity is bariatric endoscopic gastroplasty (gve), which offers a less invasive approach with fewer complications. however, the weight loss achieved through this technique is generally lower than that achieved with traditional bariatric surgery, leaving the impact on patients' quality of life uncertain. the aim of this multicentre exploratory descriptive study is to investigate the perception of the quality of life of patients with obesity undergoing gve, conducted at the complex operative unit of surgical digestive endoscopy of the university policlinico Agostino Gemelli IRCCS foundation as the promoting centre. italian patients over 18 years old, in post-gve follow-up for at least six months, with access to and familiarity with a computer or tablet will be included. data will be collected via a single semi-structured interview on microsoft teams, audio recorded and transcribed in full, and analysed using nvivo v1.6.2.32. participants' statements will be categorised into semantic categories and subsequently refined into sub-themes and themes through an iterative process.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age: Patients older than 18 years.
  • Treatment: Patients who have undergone GVE surgery and have been in post- surgery for at least six months.
  • Access and technological competence: Patients who have a computer or tablet at home and are familiar with their use.
  • Informed consent: Patients who are able to understand and give informed consent informed consent to participate in the study.
  • Language comprehension: Patients who have a good understanding of the language Italian language, both written and spoken, to ensure correct completion and understanding of the informed consent and the study instructions.

Exclusion criteria

  • Patients who have been enrolled in experimental studies involving additional procedures during GVE will be excluded

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

0

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Central trial contact

Chiara Massari

Data sourced from clinicaltrials.gov

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