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Self-compassion and Nutrition (SCAN) Study

Comparison of Two Approaches for Improving Long-term Weight Loss Among Individuals With Severe Obesity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04289636
Enrollment
28
Registered
2020-02-28
Start date
2020-09-01
Completion date
2021-07-13
Last updated
2021-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Weight Loss

Keywords

self-compassion, exercise, nutrition, physical activity

Brief summary

The purpose of this study is to examine the feasibility of two approaches for improving long-term weight loss success among individuals with severe obesity. All participants will receive a 15-week, standard behavioral weight loss program followed by either 8 weeks of a mindfulness self-compassion intervention or 8 weeks of a nutrition and cooking education intervention (determined via randomization procedures). Assessments of weight, physical activity, and other weight-related and psychosocial factors will occur at baseline, 4 months, 6 months, and 9 months.

Interventions

Using a combination of individual (\ 1x/month) and group-based (\ 3x/month) meetings, participants will be taught behavioral approaches for changing diet and exercise behaviors. This intervention will be 15 weeks in duration and will be delivered remotely using a video-conferencing platform.

BEHAVIORALSelf-compassion

This 8-week, group-based program will help train individuals on how to handle difficult emotions with greater ease, how to transform difficult relationships, and how to motivate and encourage oneself, rather than being self-critical.

This 8-week, group-based program will help individuals to improve the quality of their diet through nutrition education and basic cooking skills for preparing healthy meals.

Sponsors

The Miriam Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-65 years * BMI between 40 - 55 kg/m2 * Female * Score high on internalized weight bias

Exclusion criteria

* Presence of any condition that would limit one's ability to exercise (i.e., orthopedic limitations) * Recent weight loss (≥15 pounds within the past 6 months) * History of bariatric surgery * Current or recent enrollment (completed \<1 year ago) in a weight loss program at the Weight Control and Diabetes Research Center * Currently taking any weight loss or other medication that could alter one's metabolism * Women who are pregnant, planning on becoming pregnant in the next 6 months, or those pregnant within the past 6 months * Serious psychiatric disorder (e.g., psychosis, major depression, suicidality) - * Participants with a history of diabetes or heart disease will be considered for this study only if their heart disease or diabetes is well controlled, and physician consent will be required.

Design outcomes

Primary

MeasureTime frameDescription
Recruitment feasibility will be assessed by the number of participants screened and enrolledAt the end of the study, up to 9 months post-baselineRecruitment feasibility will be assessed by the number of participants screened and enrolled
Session attendance will be assessed by calculating the overall session attendance (# of sessions completed/# of sessions possible).6 monthsThe feasibility of the intervention will be assessed by calculating the overall session attendance
Acceptability of the intervention (retention) will be determined by the percentage of participants completing the 9-month assessment visit9 monthsAcceptability of the intervention (retention) will be determined by the percentage of participants completing the 9-month assessment visit

Secondary

MeasureTime frame
Percent weight change at 6 months6 months after study enrollment
Percent weight change at 9 months9 months after study enrollment

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026