Plant-based Protein-rich Weight Loss Intervention in 55+ Adults With Obesity

Recruiting now · Not applicable

Conditions studied: Obesity

In brief

The objective of the 2EAT RCT is to investigate whether a shift towards more plant-based (≥60% with a minimum of 50%) protein intake can be achieved in an energy restricted diet for three and six months in older adults (55+) with obesity. The 2EAT researchers developed a new dietary counseling plan for six months. This includes four individual consultations, five group meetings and three 24h-recalls. In these six months, participants receive dietary counseling focused on energy restriction (-500 kcal), higher protein intake (aim towards 1.2 g/kg/d, minimum of 0.8 g/kg/d). Participants are randomly allocated either to the more plant-based diet (≥60%) or the more animal-based diet (≥60%). At the start of the intervention, participants are provided with a workbook and recipe book. Secondary objectives are to assess the effect after three and six months 2EAT dietary treatment on 1) weight loss and 2) skeletal muscle mass. Exploratory objectives are to assess the effect after three and six months 2EAT dietary treatment on 1) physical health outcomes (muscle mass and physical performance), 2) body composition, 3) metabolic blood parameters, 4) vitality and quality of life, 5) nutritional intake, 6) behavioral changes, 7) evaluate the process of the dietary treatment.

Key facts

Study ID

NCT07429136

Run by

Amsterdam University of Applied Sciences

People needed

200

Starts

2024-08-13

Expected to finish

2027-04-01

Last updated by the study team

2026-02-24

Who can join

Age: 55 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Aged 55 or older
• Are obese: have a BMI of >30 kg/m2 or BMI >27 kg/m2 and waist circumference >88 cm (women) or >102 cm (men)
• Living independently (not in a health facility)
• The willingness that the general practitioner will be notified of study participation
• Written informed consent
• Willingness to comply with the protocol
• Consent of the study physician

You may not qualify if…

• Inability to understand the Dutch language
• Cognitive impairment (MMSE <15)
• Use of total or partial parenteral nutrition (TPN)
• Alcohol or drug abuse in the opinion of the investigator
• Current enrolment in a fixed rehabilitation program or other intervention studies
• Palliative treatment or a life expectancy of ≤ 3 months
• Following a vegetarian or vegan (100% plant-based) diet
• Bariatric surgery
• Active medical treatment interfering with this intervention (e.g. weight loss medication as Ozempic, cancer patients receiving systemic and immune therapy)
• Physical disabled: unable to meet the general daily exercise guideline for adults
• Planned a holiday during the intervention period and is unable to attend group- or individual sessions for > 3 weeks
• The health conditions below will be assessed by the study physician. When a condition interferes the dietary treatment or if the diet worsens the participants health it counts as exclusion criteria:
• Diagnosed with unstable coronary heart disease (CHD), decompensated heart failure, uncontrolled hypertension or uncontrolled arrhythmias (e.g. heart failure NYHA >3)
• Diagnosed degenerative neurocognitive disorders
• Diagnosed with renal failure
• COPD GOLD >3

Where it is running

• Hogeschool van Amsterdam — Amsterdam, South Holland, Netherlands (enrolling)

Full record on ClinicalTrials.gov

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