Overweight and Obesity Clinical Trial
Official title:
Kg-Free: an Acceptance, Mindfulness and Compassionate-based Intervention for Women Struggling With Their Weight: A Randomized Controlled Trial
This study aims to test the efficacy and feasibility of an acceptance, mindfulness and compassionate-based intervention for women with overweight and obesity without binge-eating disorder (Kg-Free). Kg-Free intervention comprises 10 weekly group sessions plus 2 booster fortnightly sessions (31/2months) 2h30 hours each, run in small groups at Coimbra's University Hospital. The main goal of Kg-Free intervention is to reduce weight self-stigma and unhealthy eating behaviours and promote quality-of-life by targeting weight-related experiential avoidance and self-criticism patterns. The intervention focuses on fostering a greater awareness and ability to be in contact, tolerate and accept all internal experiences (even the unwanted ones, such as craving for food, fatigue, stigma and shame), rather than trying to avoid, control or change them. Additionally, the intervention intents for participant's to develop a compassionate attitude towards themselves, especially during challenging times in order to decrease shame and self-criticism.
This project aims to develop and test the efficacy of an integrated intervention (Kg-FREE),
based on different and complementary approaches from the 3rd generation therapies
(Acceptance and commitment therapies - ACT, Mindfulness and Compassion Focused Therapy) that
have been showing promising results individually, but that were never tested simultaneously
in intervention for people struggling with their eating and weight. Moreover, the
intervention aims to act specifically on patients' self-criticism and experiential avoidance
patterns in order to reduce weight-self-stigma and promote healthy behaviours and
quality-of-life. Indeed, several studies have been suggesting the crucial role of these
emotional regulation processes on behavioural modification. This study will investigate the
impact of the changes in several psychological processes in different obesity dimensions,
such as body mass and biochemical parameters associated with health risks, eating
behaviours, stigma, health and quality of life.
The Kg-FREE intervention encloses 10 weekly group sessions (2, 5 hours/ each), highly
experiential followed by two 2 booster fortnightly sessions. The intervention is divided
into several modules, that are applied in a structured way: a) psycho education related to
eating and physical exercise healthy habits; b) how our brain works and how does this relate
to our eating and weight; c) Life values identifications to enhance intrinsic motivation; d)
cognitive fusion and experiential avoidance as maladaptive strategies that underlie the
psychological suffering, the negative affect (e.g. shame) and self-criticism; e) mindfulness
exercises as a more adaptive strategy for emotional regulation; f) development of
self-compassion as an antidote for shame and self-criticism, activating the soothing system
and deactivating the threat system.
Kg-Free sessions were carried out by a clinical psychologist with previous training in
contextual-behavioral therapies and one clinical psychology master student. The intervention
protocol was built upon pre-existent ACT and mindfulness-based protocols for people with
eating and weight issues (e.g., Forman et al., 2013; Kristeller & Wolever, 2011; Lillis et
al., 2009; Tapper et al., 2009). Additionally, and because it has been recognized the
importance of integrating compassion in behavioural interventions (e.g., Luoma & Platt,
2015), specially to deal with shame and self-criticism (Gilbert, 2010) a compassion
component was added. This component aimed at training participants to develop a more
accepting and kind relationship with themselves, particularly when things go wrong or when
facing errors or failures.
All session followed the same basic structure, starting with 30 minutes of shared
experience, followed by a five-minute mindfulness practice. Then the session content was
delivered, followed by an eating mindfulness practice to train the ability to pay attention
to food and eating physical sensations. Finally, the session content was briefly revised and
practices for the week were established (e.g., mindfulness or compassion exercises). A
participants' manual was provided, which included the targeted constructs, examples and
exercise sheets. Audio files were given to the participants to ensure the practice of
mindfulness and compassion exercises between sessions. Moreover, a Portuguese therapist
manual was also assembled and is available upon request.
Previously to data collection, ethical approval was obtained from Clinical Trials Unit from
Coimbra's University Hospital. Participants were adult women, aged between 18 and 55 years
old, with overweight or obesity (BMI ≥ 25) without binge-eating, enrolled in nutritional
treatment for weight loss in primary care units and Hospitals from Coimbra's district,
Portugal. Participants were recruited directly at the medical care units in the day of their
appointment. Participants were informed about the voluntary and confidential nature of the
data. Also, a brief overview of the treatment program was presented and participants were
required to sign the informed consent. In order to assure confidentiality a numerical unique
code was assigned to each participant.
After eligibility assessment, participants that meet inclusion criteria were randomly
assigned into one of the two study conditions - experimental group that will receive the
Kg-Free intervention and a control group that will maintain Treatment as usual (which
consisted in dietary and physical activity support), using a using a computer-based random
allocation. The study followed the principle of treatment received.
The study comprised four different assessment moments (M0, M1, M2 e M3), namely before
intervention (M0), at the end of the intervention (M1) and two follow-up moments at three
(M2) and six months (M3) after the intervention. In all assessments data regarding
participants' biochemical (lipid profile) and body mass parameters, eating behaviours,
health, stigma and quality of life as well as psychological processes was collected.
Regarding biochemical data, the blood samples were collected and analysed by the clinical
analysis laboratory from the Pharmacy department. Confidentiality was assured hence only the
research code for each participant was provided to the laboratory. All participants were
weighted with their street clothes (without shoes) using the same Body Composition Analyzer
(Tanita TBF-300) accurate to 0.1kg. Waist circumference was measured using a tape measure at
the umbilicus. The remaining data collection was carried out by clinical psychologists from
the research team (blinded to participant's treatment condition).
Statistical analysis All data analyses were performed using Statistical Package for the
Social Sciences (SPSS, V.20) and alpha level was set at .05. Independent sample t tests were
used in order to compare intervention and control groups at baseline. Power analysis for
ANCOVA was calculated at priori. Using a significance level of p<.05 and a power of 80%, a
sample size of 31 per group (N = 62) was needed to detect a standardized effect size of f =
0.40.
To test between-group differences at post-treatment ANCOVA with baseline as covariate and
condition as a fixed factor were performed. Paired samples t-tests were performed to explore
within-group differences from pre to post test, for each group separately. All effect sizes
were calculated using Cohen's d.
In a second study, Repeated Measures ANOVA was performed to test differences between
pre-treatment, post- treatment and 3month follow-up assessments for all participant's that
completed Kg-Free intervention (N = 53). Whenever sphericity assumption was violated, the
Greenhouse-Geisser correction was used to produce a valid F-ratio. Post-Hoc analyses using
Bonferroni adjustment for multiple comparisons was used to explore pairwise differences
(pre-to-post treatment; pre-to-3 months and post-to-3 months). Effect sizes were calculated
using partial eta square (ƞ2). Finally, to explore the psychological processes that underlie
the changes in health and weight and eating-related outcomes after the Kg-Free intervention
MEMORE macro (Mediation and Moderation analysis for Repeated measures designs) was used.
MEMORE allows for the estimation of total, direct, and indirect effects of independent
variable (X) on dependent variable (Y) through one or more mediators (M) simultaneously
two-occasion within-subjects design.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care
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