Overweight or ObesityNCT05248607
Lived Experience of Overweight/Obese Patients Who Have Benefited From a Mindful Eating Program.
An observational study of Overweight or Obesity, run by University Hospital, Montpellier at 1 site in France.
Trial summary
The main objective is to understand the lived experience of overweight/obese patients who have followed the mindful eating program at Montpellier University Hospital. Semi-structured face-to-face interviews will be conducted in the Nutrition-Diabetes service by using a questionnaire. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Overweight or Obesity
- How many people
- 20 participants
- Where
- 1 siteFrance
- Study dates
- 18 Feb 2022to 30 Sep 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Participants will be recruited among people who have consulted a doctor in the Nutrition-Diabetes service for overweight/obesity (BMI 25-39.9 kg/m²) and who have followed a mindful eating program led by Béatrix Toto within the service. Each program has 12 participants (2 sessions per year).
Who may be able to join
- People who have attended at least 6 out of 8 sessions of the mindful program
Who cannot join
- People who have attended less than 6 sessions of the program.
- Declining participation
Trial locations and contacts
1 site in 1 country.
Danielson Rakotoarivony contact
France1 site, 1 recruiting
- Recruiting
Uhmontpellier
Montpellier, 34295
Antoine AVIGNON, PUPH, 4 67 33 84 02 ext. 33, a-avignon@chu-montpellier.fr
About this study
Official title: Evaluation of the Lived Experience of Overweight/Obese Patients Who Have Benefited From a Mindful Eating Program at Montpellier University Hospital by Semi-structured Face-to-face Interviews.
The main objective is to understand the lived experience of overweight/obese patients who have followed the mindful eating program at Montpellier University Hospital. Semi-structured face-to-face interviews will be conducted in the Nutrition-Diabetes service by using a questionnaire.
- Conditions
- Overweight or Obesity
- Medical subject headings
- Overweight, Obesity
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of participants with the lived experience
the experience of overweight/obese patients who have followed the current mindful eating program at Montpellier University Hospital.
Measured: day 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Feb 2022
- Study start18 Feb 2022
- Primary completion1 Sep 2022 (estimated)
- Study completion30 Sep 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Overweight or ObesityStudies of the same condition, open and under way.
- More trials run by University Hospital, MontpellierThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Retrospective
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Montpellier
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Marion Van Beekum, resident, Principal investigator, University Hospital, Montpellier
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05248607
- Sponsor's protocol ID
- RECHMPL22_0073
- Status last verified
- Apr 2022
- First submitted
- 7 Feb 2022
- Last updated
- 14 Apr 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: NC
Study at a glance
From the registry record, last updated by the sponsor on 14 Apr 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Lived Experience of Overweight/Obese Patients Who Have Benefited From a Mindful Eating Program at Montpellier University Hospital by Semi-structured Face-to-face Interviews.
- ClinicalTrials.gov ID
- NCT05248607
- Acronym / sponsor ID
- RECHMPL22_0073
- Conditions
- Overweight or Obesity
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- University Hospital, MontpellierUniversity, hospital or other
- Study start
- 18 Feb 2022 (actual)
- Primary completion
- 1 Sep 2022 (estimated)
- Study completion
- 30 Sep 2022 (estimated)
- First posted
- 21 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The main objective is to understand the lived experience of overweight/obese patients who have followed the mindful eating program at Montpellier University Hospital. Semi-structured face-to-face interviews will be conducted in the Nutrition-Diabetes service by using a questionnaire.
Study design
- Observational model
- Other
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Participants will be recruited among people who have consulted a doctor in the Nutrition-Diabetes service for overweight/obesity (BMI 25-39.9 kg/m²) and who have followed a mindful eating program led by Béatrix Toto within the service. Each program has 12 participants (2 sessions per year).
Key inclusion criteria (1 listed)
- People who have attended at least 6 out of 8 sessions of the mindful program
Key exclusion criteria (2 listed)
- People who have attended less than 6 sessions of the program.
- Declining participation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Number of participants with the lived experience
Time frame: day 1
the experience of overweight/obese patients who have followed the current mindful eating program at Montpellier University Hospital.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Apr 2022.
- Individual participant dataSharing planned: Undecided. NC
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Danielson Rakotoarivony contact
Marion Van Beekum, resident principal investigator
University Hospital, Montpellier
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Overweight or Obesity, run by University Hospital, Montpellier at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 14 Apr 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Antoine AVIGNON, Pu-Ph (04 67 33 84 02 ext. 33, a-avignon@chu-montpellier.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of participants with the lived experience (time frame: day 1). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Apr 2022.