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RecruitingNCT06617689BAR-VANNTANNUpdated Jul 20, 2026

Effect of Patient Education on Drinking Behaviour and Oral Hygiene in Patients Undergoing Bariatric Surgery

An interventional study of Various levels of patient education in Obesity and Bariatric Surgery Candidate, sponsored by St. Olavs Hospital. Recruiting at 1 site in Norway. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-20.

Sponsored by St. Olavs Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started Jan 2025; still recruiting 1 year 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The background for the study is that many bariatric surgery patients struggle with their oral health after bariatric surgery. This is probably related to both physiological changes and changes in eating and drinking patterns. In addition, many have reduced oral health even before surgery, and a significant proportion also have dental treatment anxiety, which also affects their ability to seek dental treatment. In sum, this is probably a patient group that may be at risk of oral pathology.

Participants in the study will be randomly allocated to different patient education programmes. The three interventions are:

  1. customised information on a website
  2. education delivered by a clinician
  3. distribution of free samples relevant to dental hygiene

The outcomes recorded are level of knowledge, drinking patterns, self-perceived oral health, and oral hygiene routines.

Read the detailed description

Both caries and periodontitis are more prevalent among people with obesity. At the same time, we know that bariatric surgery is associated with poorer oral health expressed by caries, enamel erosion and short-term increased inflammation in the gums. Although we do not yet have evidence to determine causality, we suspect that oral health in bariatric surgery patients is further impaired by both systemic effects (hyposalivation, altered oral microbiome, reflux and vomiting) and by altered eating and drinking patterns after surgery (acid exposure with subsequent demineralisation of tooth enamel).

The patient's own diet and oral hygiene can be an opportunity to prevent or slow down such oral problems, but requires personal effort and must be a special focus in patient education.

Patient education is one of the hospital's statutory duties, but the quality of patient education is rarely systematically investigated. This project investigates the effect of three alternative educational interventions on patients' drinking habits, oral hygiene routines, knowledge level and oral health. The three interventions are a website with adapted patient information, group-based education given by healthcare professionals, and distribution of relevant product samples to maintain oral hygiene. Patients are randomised between the different educational interventions.

02

Conditions studied

  • Obesity
  • Bariatric Surgery Candidate

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Keywords

  • Obesity
  • Oral health
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,692 are open to participants now.

This study's planned enrollment of 300 is above the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

St. Olavs Hospital is the lead sponsor of 165 studies on the registry; 30 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

Inclusion criteria

  • Eligible for bariatric surgery at a Norwegian hospital

Exclusion criteria

Exclusion Criteria:

  • Insufficient language skills
  • Lack of consent competency
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    Arm 1: Group-based teaching

    In this arm, all three educational activities are included: Teaching (in a group), distribution of free dental hygiene samples, and advice on reading the customised website. This arm is compared to Arm 2.

    Other: Various levels of patient education

  • Active comparator
    Arm 2: Comparator to Arm 1

    In this arm, patients are distributed free dental hygiene samples, and given advice on reading the customised website. This arm is compared to Arm 1.

    Other: Various levels of patient education

  • Experimental
    Arm 3: Goodiebag

    In this arm, patients are distributed free dental hygiene samples, and given advice on reading the customised website. This arm is compared to Arm 4.

    Other: Various levels of patient education

  • Active comparator
    Arm 4: Comparator to Arm 3

    In this arm, patients are adviced on reading the customised website. This arm is compared to Arm 3.

    Other: Various levels of patient education

Interventions

  • OtherVarious levels of patient education

    The three interventions: GROUP BASED TEACHING In groups of 8-12 patients, 30 minutes of standardised teaching is given. The teaching focuses in particular on the changes in diet and the impact this has on oral pH, enamel erosion and caries; recommended oral hygiene; and good drinking habits. WEBSITE Website providing recommendations for oral hygiene and drinking habits, as well as in depth information on the topic. DENTAL HYGIENE SAMPLES These are samples relevant for maintaining proper oral hygiene, distributed free, together with a description of how to use them.

06

What researchers measure

Primary outcomes

  1. Drinking habits

    Reported intake plain water with no additives

    Time frame: Baseline to 6 months postop. to 24 months postop.

Secondary outcomes

  1. Dental hygiene

    Self-reported dental hygiene

    Time frame: Baseline to 6 months postop. to 24 months postop.

  2. Level of knowledge

    Knowledge reflecting the central parts of the patient education

    Time frame: Baseline to 6 months postop. to 24 months postop.

Other outcomes

  1. Oral health

    Self-reported oral health, including OHIP14

    Time frame: Baseline to 6 months postop. to 24 months postop.

07

Study locations

1 of 1 sites recruiting
  • St. Olavs hospital
    Trondheim, Norway
    • Magnus Strømmen · Contact
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06617689
Lead sponsor
St. Olavs Hospital
Collaborators
Helse Møre og Romsdal Hospital Trust, Helse Nord-Trøndelag HF, Oslo University Hospital
Responsible party
Sponsor
First posted
Sep 27, 2024
Start date
Jan 28, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Jul 20, 2026

Study contacts

Magnus N Strømmen
Contact
magnus.strommen@stolav.no
+4791701010
Magnus N Strømmen
principal investigator · St. Olavs Hospital

Oversight

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

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