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Use of Chewing Gum to Facilitate Appetite Control and Weight Loss

Use of Chewing Gum to Facilitate Appetite Control and Weight Loss in Overweight Individuals Treated by Lifestyle Modification

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00871676
Enrollment
146
Registered
2009-03-30
Start date
2006-05-31
Completion date
2009-12-31
Last updated
2016-08-17

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

Conditions

Obesity, Overweight

Brief summary

This purpose of this study was to test the use of chewing gum as an adjunct to lifestyle modification to facilitate appetite control and weight loss in overweight and obese individuals.

Interventions

BEHAVIORALLifestyle modification

16 weekly followed by 8 monthly group behavioral weight loss sessions.

BEHAVIORALLifestyle modification plus gum

16 weekly followed by 8 monthly group behavioral weight loss sessions. Subjects were also given gum along with instructions for times and occasions to chew with the aim of facilitating weight loss and appetite control.

Sponsors

St. Luke's-Roosevelt Hospital Center
CollaboratorOTHER
University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* 21-75 years of age * Body Mass Index of 25-45 inclusive

Exclusion criteria

* major medical psychiatric conditions * medications know to effect weight * full or partial dentures * 18 or fewer teeth * regular gum chewing (≥ 2 pieces/day) * use of any tobacco product * sensitivity to the following ingredients (mint, magnolia bark, eggs, or English Muffins) * history of PKU * sensitivity or allergy to aspartame * current/history of alcohol abuse or addiction (within 5 year) * recreational drug use * recent significant weight change (+/- 5% in previous 6 months) * currently pregnant or nursing and willingness not to get pregnant during course of study * participation in any other research studies * proximity to clinic (within one hour) * access to reliable transportation

Design outcomes

Primary

MeasureTime frame
Weight lossWeek 16 and 52

Secondary

MeasureTime frame
Appetite controlWeeks 4, 8, 12, 16 and 52

Countries

United States

Outcome results

None listed

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