Efficacy of Telephone-Based Cognitive Behavioral Therapy for Weight Loss, Disordered Eating, and Psychological Distress After Bariatric Surgery

Author:

Sockalingam Sanjeev1234,Leung Samantha E.1,Ma Clement35,Tomlinson George6,Hawa Raed124,Wnuk Susan124,Jackson Timothy17,Urbach David18,Okrainec Allan1,Brown Jennifer9,Sandre Daniella9,Cassin Stephanie E.2410

Affiliation:

1. Bariatric Surgery Program, University Health Network, Toronto, Ontario, Canada

2. Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada

3. Centre for Addiction and Mental Health, Toronto, Ontario, Canada

4. Centre for Mental Health, University Health Network, Toronto, Ontario, Canada

5. Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada

6. Institute of Health Policy, Management and Evaluation, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada

7. Division of General Surgery, University Health Network, University of Toronto, Toronto, Ontario, Canada

8. Department of Surgery, Women’s College Hospital, Toronto, Canada

9. Ottawa Hospital Bariatric Centre of Excellence, Ottawa, Ontario, Canada

10. Department of Psychology, Toronto Metropolitan University, Toronto, Ontario, Canada

Abstract

ImportanceWeight regain after bariatric surgery is associated with recurrence of obesity-related medical comorbidities and deterioration in quality of life. Developing efficacious psychosocial interventions that target risk factors, prevent weight regain, and improve mental health is imperative.ObjectiveTo determine the efficacy of a telephone-based cognitive behavioral therapy (tele-CBT) intervention at 1 year after bariatric surgery in improving weight loss, disordered eating, and psychological distress.Design, Setting, and ParticipantsThis multisite randomized clinical trial was conducted at 3 hospital-based bariatric surgery programs, with recruitment between February 2018 and December 2021. Eligibility for participation was assessed among 314 adults at 1 year after bariatric surgery who were fluent in English and had access to a telephone and the internet. Patients with active suicidal ideation or poorly controlled severe psychiatric illness were excluded. Primary and secondary outcome measures were assessed at baseline (1 year after surgery), after the intervention (approximately 15 months after surgery), and at 3-month follow-up (approximately 18 months after surgery). Data were analyzed from January to February 2023.InterventionsThe tele-CBT intervention consisted of 6 weekly 1-hour sessions and a seventh booster session 1 month later. The control group received standard postoperative bariatric care.Main Outcomes and MeasuresThe primary outcome was postoperative percentage total weight loss. Secondary outcomes were disordered eating (Binge Eating Scale [BES] and Emotional Eating Scale [EES]) and psychological distress (Patient Health Questionnaire-9 item scale [PHQ-9] and Generalized Anxiety Disorder-7 item scale [GAD-7]). The hypotheses and data-analytic plan were developed prior to data collection.ResultsAmong 306 patients 1 year after bariatric surgery (255 females [83.3%]; mean [SD] age, 47.55 [9.98] years), there were 152 patients in the tele-CBT group and 154 patients in the control group. The group by time interaction for percentage total weight loss was not significant (F1,160.61 = 2.09; P = .15). However, there were significant interactions for mean BES (F2,527.32 = 18.73; P < .001), EES total (F2,530.67 = 10.83; P < .001), PHQ-9 (F2,529.93 = 17.74; P < .001), and GAD-7 (F2,535.16 = 15.29; P < .001) scores between the tele-CBT group and control group across all times.Conclusions and RelevanceThis study found that tele-CBT delivered at 1 year after surgery resulted in no change in short-term weight outcomes but improved disordered eating and psychological distress. The impact of these psychosocial improvements on longer-term weight outcomes is currently being examined as part of this longitudinal multisite randomized clinical trial.Trial RegistrationClinicalTrials.gov Identifier: NCT03315247

Publisher

American Medical Association (AMA)

Subject

General Medicine

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