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The INFINITE Study: A Prospective Investigation of a Nutrient-dense Diet in Early Addiction Recovery

The INFINITE Study: A Prospective Investigation of a Nutrient-dense Diet in Early Addiction Recovery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04030858
Enrollment
125
Registered
2019-07-24
Start date
2019-09-03
Completion date
2021-08-31
Last updated
2019-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Addiction, Mental Health Issue

Brief summary

The trial will be placed within an ongoing addiction recovery program at Infinite Recovery in Austin, TX. Members with any addiction enrolling in an inpatient treatment program at Infinite Recovery will be recruited into this 1-year study to evaluate the effectiveness of a plant-based diet to aid drug and/or alcohol addiction recovery. Volunteers willing to participate in the trial will be randomly assigned to a treatment or control group. Those in the treatment group will follow the standard protocol offered by Infinite Recovery, with the exception that they will be provided with only plant-based meals. Both groups will also receive nutrition education to support their dietary plan. Several health and wellbeing endpoints will be assessed as part of the standard care at Infinite Recovery, combined with a few additional measurements described within this study protocol.

Interventions

BEHAVIORALPlant-based diet + nutrition education

The intervention group will adopt a nutrient-dense dietary pattern and receive nutrition education sessions specific to that lifestyle. The diet protocol is comprised of minimally-processed plant foods such as fruits, vegetables, legumes, beans, nuts and seeds. No refined sugars, added salt, or oil will be included. Dietary fat intake limited to 20% of total calories or less per day. Animal products will be eliminated. This dietary pattern is expected to improve resilience, mood, inflammation, microbiome, spirituality, and overall general health (as measured by weight, cholesterol, blood pressure). The treatment group will also receive weekly nutrition education sessions to support the diet.

Sponsors

Northern Arizona University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This is a randomized controlled trial with an intervention and control group comparison.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 18 or older * Entering inpatient treatment at Infinite Recovery Addiction Treatment Facility

Exclusion criteria

* Pregnant * Psychiatrically unstable.

Design outcomes

Primary

MeasureTime frameDescription
ResilienceChange from baseline to week 3Measured by the Connor-Davidson Resilience Scale (CD-RISC); scale scores range 0-100, with higher values representing better outcomes.

Contacts

Primary ContactTara Kemp, BA
tk479@nau.edu7249726224
Backup ContactJay Sutliffe, PhD
jay.sutliffe@nau.edu928-523-7450

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026