# Beyond Weight Loss: Holistic Impacts of a Digital Weight Management Programme Integrating Tirzepatide

**Authors:** Lena M Sikorska, Vivian N Liu, Hans Johnson, Earim Chaudry, Daniel Reisel, Ashley K Clift, David R Huang

PMC · DOI: 10.7759/cureus.102817 · Cureus · 2026-02-02

## TL;DR

A digital weight management program using tirzepatide led to significant weight loss and improvements in mental health and metabolic markers over 12 months.

## Contribution

Demonstrates real-world effectiveness of a digital program integrating tirzepatide for weight loss and broader health outcomes.

## Key findings

- Participants achieved a mean 22.7% weight loss after 12 months.
- Significant reductions in binge eating and depression scores were observed.
- Metabolic improvements included lower blood pressure and normalized HbA1c in prediabetic individuals.

## Abstract

Introduction

Recent pharmacological advancements, such as tirzepatide, a dual GIP/GLP-1 receptor agonist, offer new therapeutic options, delivering substantial weight loss with potential mental health and well-being benefits. Digital weight loss services (DWLS) that combine anti-obesity medication with nutritional and behavioural support are increasingly used, but real-world evidence remains limited as clinical trial outcomes may not reflect routine practice. This service evaluation assessed 12-month outcomes of individuals enrolled in Voyager, a pilot programme delivered by the Voy DWLS.

Methods

UK residents (n=60) aged 18-65 with body mass index (BMI) ≥30 kg/m², naive to prior anti-obesity medication. Participants attended the Voyager programme between July 2024 and August 2025, comprising tirzepatide treatment and digital interventions (health coaching, side effects tracking, clinical support, app access, and webinars). The primary outcome was the percentage total body weight loss (WL) from baseline to 12 months. Secondary outcomes included anthropometric measures, patient-reported outcomes (Binge Eating Scale (BES) and Patient Health Questionnaire-9 (PHQ-9) scores), blood pressure, side effects, and laboratory results. Statistical analyses employed descriptive statistics, paired t-tests, and linear mixed-effects models.

Results

Participants were predominantly female (90%, n=54), with a mean age of 44.6±11.1 years and baseline BMI of 37.1±6.2 kg/m². At 12 months, mean WL reached 22.7% (95% CI 20.92-24.48; p<0.001). Waist and hip circumference, and waist-to-hip ratio, declined significantly. BES scores fell by 18 points (95% CI 14.5-21.67) and PHQ-9 by 3.06 points (95% CI 2.26-3.87). Mean systolic and diastolic blood pressure decreased by 9.07 mmHg (95% CI 5.52-12.61) and 4.90 mmHg (95% CI 2.53-7.26), respectively (all p<0.001). Nausea was the most common side effect and decreased over time. Significant longitudinal improvements occurred across cardiometabolic markers, including glycated haemoglobin (HbA1c), low-density lipoprotein (LDL) cholesterol, total cholesterol, and cholesterol/high-density lipoprotein (HDL) ratio; all five participants with prediabetes normalised HbA1c by 12 months.

Conclusion

The Voyager programme integrating tirzepatide achieved clinically meaningful weight loss and broad metabolic and psychological improvements over 12 months, supporting integrated pharmacological-digital approaches to obesity care.

## Linked entities

- **Chemicals:** tirzepatide (PubChem CID 163285897)
- **Diseases:** obesity (MONDO:0011122), prediabetes (MONDO:0006920)

## Full-text entities

- **Genes:** GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** fatigue (MESH:D005221), functional (MESH:D003291), Constipation (MESH:D003248), diarrhoea (MESH:D003967), stroke (MESH:D020521), thyroid disease (MESH:D013959), weight gain (MESH:D015430), fatty liver disease (MESH:D005234), type 1 or type 2 diabetes mellitus (MESH:D003924), obstructive sleep apnoea (MESH:D020181), Obesity (MESH:D009765), depression (MESH:D003866), chronic back pain (MESH:D059350), Nausea (MESH:D009325), osteoarthritis (MESH:D010003), hypertension (MESH:D006973), PCOS (MESH:D011085), coronary heart disease (MESH:D003327), renal or hepatic impairment (MESH:D008107), headache (MESH:D006261), binge eating disorder (MESH:D056912), prediabetes (MESH:D011236), Binge Eating (MESH:D002032), WL (MESH:D015431), asthma (MESH:D001249), cardiovascular disease (MESH:D002318), cancers (MESH:D009369), gastrointestinal (MESH:D005767)
- **Chemicals:** Lipid (MESH:D008055), Iron (MESH:D007501), cholesterol (MESH:D002784), alcohol (MESH:D000438), Free T4 (-), T4 (MESH:D013974)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958089/full.md

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Source: https://tomesphere.com/paper/PMC12958089