2026-04-30T03:51:00Zhttps://repisalud.isciii.es/rest/oai/requestoai:repisalud.isciii.es:20.500.12105/228722024-11-28T20:46:32Zcom_20.500.12105_15322com_20.500.12105_2051col_20.500.12105_16967
Repisalud
author
Owens, Matthew
author
Watkins, Edward
author
Bot, Mariska
author
Brouwer, Ingeborg Annemarie
author
Roca, Miquel
author
Kohls, Elisabeth
author
Penninx, Brenda
author
van Grootheest, Gerard
author
Cabout, Mieke
author
Hegerl, Ulrich
author
Gili, Margalida
author
Visser, Marjolein
author
MooDFOOD Prevention Trial
2024-09-13T09:11:46Z
2024-09-13T09:11:46Z
2020
Owens M, Watkins E, Bot M, Brouwer Ingeborg A, Roca M, Kohls E, et al. Acceptability and feasibility of two interventions in the MooDFOOD Trial: a food-related depression prevention randomised controlled trial in overweight adults with subsyndromal symptoms of depression. BMJ Open. 2020;10(9):e034025.
10.1136/bmjopen-2019-034025
2044-6055
BMJ Open
http://hdl.handle.net/20.500.13003/12208
32933954
L632853128
2-s2.0-85091052159
https://hdl.handle.net/20.500.12105/22872
573829200004
Objectives: We report on the acceptability, feasibility, dose-response relationship and adherence of two nutritional strategies to improve mood (multinutrient supplements; food-related behavioural activation (F-BA)) studied in a randomised controlled depression prevention trial (the Multi-country cOllaborative project on the rOle of Diet, Food-related behaviour, and Obesity in the prevention of Depression (MooDFOOD) Trial). We also assessed baseline determinants of adherence and assessed whether better adherence resulted in lower depressive symptoms. Design: Randomised controlled trial with a 2x2 factorial design conducted between 2015 and 2017. Setting Germany, the Netherlands, UK and Spain. Participants: Community sample of 1025 overweight adults with elevated depressive symptoms without a current episode of major depressive disorder. Main eligibility criteria included age (18-75 years), being overweight or obese, and having at least mild depressive symptoms, shown by a Patient Health Questionnaire Score of >= 5. A total of 76% of the sample was retained at the 12-month follow-up. Interventions Daily nutritional supplements versus pill placebo or an F-BA therapy, delivered in individual and group sessions versus no behavioural intervention over a 1-year period. Primary and secondary outcome measures Primary outcome: self-reported acceptability of the interventions. Secondary outcomes: adherence and self-reported depressive symptoms. Results Most participants reported that the F-BA was acceptable (83.61%), feasible to do (65.91%) and would recommend it to a friend (84.57%). Individual F-BA sessions (88.10%) were significantly more often rated as positive than group F-BA sessions (70.17%) and supplements (28.59%). There were statistically significant reductions in depressive symptoms for those who both adhered to the F-BA intervention and had a history of depression (B=-0.08, SE=0.03, p=0.012) versus those who had no history of depression. Supplement intake had no effect on depressive symptoms irrespective of adherence. Conclusions: F-BA may have scope for development as a depression prevention intervention and public health strategy but further refinement and testing are needed.
eng
Depression & mood disorders
Nutrition & dietetics
Preventive medicine
Mental health
Clinical trials
Acceptability and feasibility of two interventions in the MooDFOOD Trial: a food-related depression prevention randomised controlled trial in overweight adults with subsyndromal symptoms of depression
research article