How Does Bariatric Surgery Affect Social Experiences and Well-being - The BaSES-study (BaSES)

November 18, 2025 updated by: Jøran Hjelmesæth, The Hospital of Vestfold

How Gastric Bypass and Sleeve Gastrectomy Change Social Experiences and Biomarkers of Well-being

Nonrandomized controlled trial to assess whether or not sleeve gastrectomy (SG) or Roux-en-Y gastric bypass (RYGB) affect social experiences and biomarkers of well-being 6 weeks and 1 year after surgery. The decision whether SG or RYGB will be performed is determined by medical decision making. Hypotheses: Bariatric surgery influences social experiences and well-being through changes in body image, reward responsivity and gut hormones. These changes may differ between gastric bypass (RYGB) and sleeve gastrectomy (SG).

Study Overview

Detailed Description

Explanation for choice of comparators

Obesity is one of the world's most serious public health problems. Conservative weight reduction methods alone (diet, exercise) often show disappointing results, as the majority of people who lose weight regain it after a shorter or longer period of time. The currently most effective measure to achieve a durable weight-loss is bariatric surgery.

When investigating the effectiveness of bariatric surgery, the focus has most often been on weight loss and obesity-related complications, while effects on social interaction and subjective experience have received much less attention. A large body of evidence has demonstrated that (supportive) social relationships benefit health. Individuals with low compared to those with high levels of social connectedness are more likely to die prematurely; and social relationships can also affect a range of other health conditions such as cardiovascular disease, cancer, and immune function. Importantly, individuals with obesity may experience social interactions as less positive than normal-weight individuals. They recount avoiding social events and relationships, but also career opportunities, shopping and other activities where they feel observed because of weight stigma. Such avoidance behavior can lead to a "chronic disengagement" with many aspects of social life, which in turn might decrease interpersonal skills. Further investigations into the link between social behavior and eating found that greater emotional eating is associated with greater social avoidance. Eating was described a means to cope with loneliness on the one hand, while on the other hand aggravating feelings of being alone due to the stigma associated with obesity. This way, loneliness and obesity can create a vicious circle. In terms of how bariatric surgery influences social interactions, one 10-year follow up study found improvements in social interactions for bariatric surgery, but not for conventional weight loss treatment. In qualitative studies, many participants mentioned that they received more positive social feedback following bariatric surgery, and that they enjoyed social activities more than before, although they also describe ambiguous feelings.

The present study will investigate whether and how two types of bariatric surgery improve the response to a range of social aspects of patients' daily lives. Further, it aims to determine potential mechanisms leading to these effects, namely changes in body image, gut hormones, and reward responsivity.

Study Type

Interventional

Enrollment (Estimated)

113

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Vestfold
      • Tønsberg, Vestfold, Norway, 3103
        • Morbid Obesity Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • scheduled for bariatric surgery and eligible for sleeve gastrectomy or gastric bypass
  • able to give consent
  • understand written and spoken Norwegian

Exclusion Criteria:

  • pregnancy and breast-feeding
  • chronic disease (endocrine, heart, neurological, lung, gastrointestinal, kidney)
  • cancer
  • acute psychotic episode

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Gastric bypass
In Roux-en-Y gastric bypass (RYGB), the left crus will be dissected free, any hiatal hernia left in place. The minor curvature is opened at the second vessel and the lesser sac entered. A 25 mL gastric pouch will be created by firing one horizontal and two vertical staple loads. The ligament of Treitz is then identified and a proximal loop of small intestine anastomosed to the pouch 60 cm from the ligament of Treitz with one linear stapler (full length of the stapler), creating an antecolic, antegastric alimentary limb. The opening will be closed using a single row, running absorbable suture. An entero-enteroanastomosis will be made 120 cm distal of the gastro-enteroanastomosis. The introductory opening is closed with a single row, running absorbable suture. The small intestine will be divided with one load between the gastro-entero-enteroanastomosis and the entero-enteroanastomosis in order to complete a bypass with an alimentary limb of 120 cm and a biliopancreatic limb of 60 cm.
Active Comparator: Sleeve gastrectomy
In sleeve gastrectomy (SG) a large part (80%) of the ventricle is removed. The greater curvature will be dissected free starting 4-5 cm from the pylorus up to the angle of Hiss. The left crus is then visualized and inspected for hiatal hernia. Small sliding hernias and wide hiatus are left in situ. The ventricle will then be lifted and any adhesions in the lesser sac divided. A 35 Fr bougie is placed down to the pylorus guiding the creation of a tubular sleeve with linear staplers. The first two loads are always green or purple, while blue or tan loads are used for the rest of the ventricle. The last stapler is placed 5 mm laterally to the angle of Hiss. The staple line will then be inspected and secured with clips for additional haemostasis, no oversewing or buttressing material is routinely used.
Experimental: Single anastomosis sleeve ileal (SASI) bypass
Exploratory small arm with a small number of particpants
The SASI bypass will performed with a similar entry of the abdominal cavity. A 6-port set up and a liver retractor is utilized. The small bowel is measured 300cm from the ileocecal valve, in sequences of 10cm, with the small bowel stretched and markers placed on the graspers, and connected to the antrum of the stomach with a 45mm stapler. The anastomosis is positioned slightly ventral on the antrum. The antrum is opened ventrally 5 cm proximal to the pylorus, just below the horizontal axis of canalis pylori. A 12 mm port positioned left to the midline is used for introduction of the stapler, which is directed distally from the patient's left to right side. 2.5 cm of the 45 mm stapler device is used for firing the anastomosis, which is completed with a 2-0 PDS running suture. The fascia defect is closed for the port where the specimen is extracted. The mesenteric defect is not closed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
1-year changes in Social Experience
Time Frame: Change from 4 weeks before surgery to 1 year after surgery
10-item checklist assessing frequency and quality of daily social interactions (preprint in August 2025: https://osf.io/preprints/psyarxiv/6psar_v2); 2 sub-scales: (1) Being with others, (2) Being alone; the diary will be filled in 14 days in a row at the end of the day. Scale (1) was designed to measure enjoyment of being with others and the duration of social contact (6 items, range: 4 to 62.4), higher values indicate more enjoyment and a higher frequency of social contact. Scale (2) was designed to measure enjoyment of being alone (3 items, range: -5 to 20), higher values here indicate more enjoyment of being alone. An additional item at the beginning of the checklists asks how many people the respondent has had social contact with during the day (5 categories).
Change from 4 weeks before surgery to 1 year after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in affect ratings after social evaluation (inclusion and exclusion)
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Positive and Negative Affect Schedule (PANAS): The PANAS is a self-report measure that is made up of two mood scales of 10 adjectives each, one measuring positive affect and the other one measuring negative affect. (1) Positive Affect Scale (range: 10-50; higher values indicate higher positive affect); (2) Negative Affect Scale (range: 10-50, higher values indicate higher negative affect)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in experience ratings after social evaluation (inclusion and exclusion)
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Need-Threat Scale: 4 sub-scales: (1) Belonging, (2) Self-Esteem, (3) Meaningful existence, (4) Control; range: 3-27 per sub-scale; higher values indicate more belonging, higher self-esteem, higher meaningful existence, and more control)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in pleasantness ratings in response to touch stimulation on the forearm
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Subjective ratings on a digitally presented visual analogue scale (VAS) scale: range 0-100 (unpleasant - pleasant) after a touch stimulation to the forearm (repeated 10 times)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in pleasantness ratings in response to self-stroking on the forearm
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Subjective ratings on a digitally presented VAS scale: range 0-100 (unpleasant - pleasant), after participants made 10 back-and-forth strokes on their forearm with their hand
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in intensity ratings in response to touch stimulation on the forearm
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Subjective ratings on a digitally presented VAS scale: range 0-100 (not intense - intense), after a touch stimulation to the forearm (repeated 10 times)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in intensity ratings in response to self-stroking on the forearm
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Subjective ratings on a digitally presented VAS scale: range 0-100 (not intense - intense), after participants made 10 back-and-forth strokes on their forearm with their hand
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in cortisol levels from hair samples
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Cortisol (in pg/mg)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in endocannabinoid levels from hair samples
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Endocannabinoids (in pg/mg)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in fasting ghrelin levels from blood samples
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Ghrelin (in pg/ml)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in body image
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaires: Appearance Evaluation Scale (AES) and the Body Areas Satisfaction Scale (BASS) - the AES was designed to measure overall satisfaction/dissatisfaction with one's appearance and physical attractiveness. It has 7 items (range: 5-35) with high scores indicating body satisfaction and low scores indicating body dissatisfaction. The BASS was designed to measure the degree of dissatisfaction-satisfaction with specific body areas and attributes (range: 9-45). Higher scores indicate greater body satisfaction and lower scores indicate greater body dissatisfaction.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in reward responsivity
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaire: Temporal Experience of Pleasure Scale (TEPS) - the TEPS was designed to measure individual trait dispositions in both anticipatory and consummatory experiences of pleasure. It consists of 18 items, of which 10 form the (1) anticipatory pleasure scale (range: 10-60), and (2) 8 items for the consummatory pleasure scale (range: 8-48). Higher values on (1) indicate enhanced reward responsiveness and imagery, while higher values on (2) indicate higher openness to different experiences and appreciation of positive stimuli.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in interoceptive ability
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaire: Body Awareness Questionnaire (BAQ) - the BAQ was designed to assess self-reported attentiveness to normal nonemotive body processes, such as sensitivity to body rhythms, ability to detect small changes in normal bodily functioning, and one's ability to anticipate bodily reactions. It consists of 18 items (range: 18-126). Higher values indicate a higher sensitivity and awareness of one's bodily states.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in belongingness
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaires: The Social Connectedness Scale Revised (SCS-R) and the Social Assurance Scale (SAS). The SCS-R was designed to measure a psychological sense of belonging, or how individuals cognitively construe interpersonal closeness with others in their social world. It consists of 20 items (range: 20-120), with higher values indicating a higher sense of belonging. The SAS was designed to measure the importance of assurance from one's social group.It consists of 8 items (range: 8-48), with higher values indicating a higher need for social assurance.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in social network size
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaire: The Social Network Index (SNI) - the SNI was designed to measure three aspects of one's social networks: (1) network diversity, (2) number of people in the network, and (3) number of embedded networks. Each of the three sub-scales is assessed on 12 items. (1) refers to the number of high-contact roles (range: 0-12), with higher values indicating a higher number of social roles. (2) refers to the total number of people with whom the respondent has regular contact, which will be summed for the 12 items (range: 0-70). Higher numbers indicate more people in one's network (to not inflate the number, items 4-12 will be scored with 7 in case the reported number of people in this group is equivalent or larger to 7). The embedded network scale (3) reflects the number of different network domains in which a respondent is active (range: 0-8), with higher numbers indicating activity in more network domains.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in self-reported eating patterns
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaire:The Three Factor Eating Questionnaire -R 21 (TFEQ-R21) measures eating behaviour and has been validated for use in individuals with obesity and will be used in the study. It consists of 21 items comprising three domain scores; (1) uncontrolled eating; assessing the tendency to lose control over eating when feeling hungry or when exposed to external stimuli, (2) cognitive restraint; assessing the conscious restriction of food intake to control body weight or body shape, and (3) emotional eating; assessing overeating related to negative mood states. The domain scores were transformed to 0-100 scales to facilitate comparison; a higher score indicates more uncontrolled, restraint, or emotional eating.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in symptoms of depression and anxiety
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaire: Hospital Anxiety and Depression Scale (HADS). The validated generic HADS measures symptoms of anxiety and depression using 14 items scored from 0-3 It is decomposed into two domains measuring depression (HADS-D) and anxiety (HADS-A), both consisting of seven items yielding a score from 0-21.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in Health Related Quality of Life 1
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Generic questionnaire: Short Form-36 Health Survey (SF-36). Each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively. Scores for each of the 8 domains and summary scores for physical and mental health will be calculated.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in Health Related Quality of Life 2
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Questionnaire: Weight-related Symptom Measure (WRSM). The validated obesity specific WRSM measures 20 symptoms commonly related to being overweight or obese, including foot problems, joint pain, sensitivity to cold, shortness of breath, etc. using two different sets of items. The first set assesses whether or not a patient is experiencing specific symptoms, and the second set rates the level of the distress of the symptoms with values from zero ("not at all") to six ("bothers a very great deal"). The first set creates an additive scale summing symptoms from 0-20, while the second forms a symptom distress scale ranging from 0-120.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in Health Related Quality of Life 3
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Obesity specific questionnaire: The Impact of Weight on Quality of Life-Lite (IWQOL-lite). The IWQOL-Lite is a 31-item measure of weight-related quality of life. There are five domain scores (Physical Function, Self-Esteem, Sexual Life, Public Distress and Work) and a total score. Scores for all domains and total score range from 0-100, with lower scores indicating greater impairment.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Changes in self-stroking velocity
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Participants are instructed to stroke their own forearm with a velocity they experience as pleasant. The duration of 10 back-and-forth strokes over a 10 cm distance on the forearm will be measured with a stop watch. Velocity in cm/sec will be calculated thereafter.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
6-week Changes in Social Experience
Time Frame: Change from 4 weeks before surgery to 6 weeks after surgery
10-item checklist assessing frequency and quality of daily social interactions (preprint in August 2025: https://osf.io/preprints/psyarxiv/6psar_v2); 2 sub-scales: (1) Being with others, (2) Being alone; the diary will be filled in 14 days in a row at the end of the day. Scale (1) was designed to measure enjoyment of being with others and the duration of social contact (6 items, range: 4 to 62.4), higher values indicate more enjoyment and a higher frequency of social contact. Scale (2) was designed to measure enjoyment of being alone (3 items, range: -5 to 20), higher values here indicate more enjoyment of being alone. An additional item at the beginning of the checklists asks how many people the respondent has had social contact with during the day (5 categories).
Change from 4 weeks before surgery to 6 weeks after surgery
Group differences between SG and RYBG patients in the above-mentioned outcomes [1-22]
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
The above-mentioned outcomes will be tested for differences between the two surgery types.
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Body Mass Index (BMI)
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
calculated from height (in cm) and weight (in kg) as kg/m^2
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in anthropometric measures
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Waist and hip circumference (cm)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in body fat
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Body fat (in %)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in blood pressure
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Systolic and diastolic blood pressure (mm/Hg)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in lipids
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Total-cholesterol, HDL-cholesterol, LDL-cholesterol and triglycerides (all in mmol/l)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in C-reactive protein (CRP)
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
CRP (mg/L)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in blood enzymes
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
ASAT (aspartate aminotransferase), ALAT (alanine-aminotransferase), LD (lactate dehydrogenase), Gamma-GT (gamma-glutamyl transferase), ALP (alkaline phosphatase) (all in U/L)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in hemoglobin
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Hemoglobin (g/100 ml)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in ferritin
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Ferritin ((µg/L)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in weight
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Percent total weight loss (%TWL) and in kg
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in fat-free mass
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Fat-free mass (in kg)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
Change in glucose parameters
Time Frame: Change from 4 weeks before surgery to 6 weeks and 1 year after surgery
HbA1c (mmol/mol); C-peptide (nmol/l)
Change from 4 weeks before surgery to 6 weeks and 1 year after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Jøran Hjelmesæth, Professor, The Hospital of Vestfold

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 12, 2022

Primary Completion (Estimated)

December 1, 2025

Study Completion (Estimated)

June 1, 2026

Study Registration Dates

First Submitted

December 8, 2021

First Submitted That Met QC Criteria

January 12, 2022

First Posted (Actual)

January 26, 2022

Study Record Updates

Last Update Posted (Actual)

November 21, 2025

Last Update Submitted That Met QC Criteria

November 18, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-anonymized individual participant data can be made available following publication upon reasonable request to authors Jøran Hjelmesæth and Uta Sailer. Data will be shared according to the consent given by the participants and Norwegian laws and legislation.

IPD Sharing Time Frame

For at least 10 years after publication

IPD Sharing Access Criteria

All requests must be handled within the legal framework of Norway; non-commercial use of de-anonymized data

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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