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A Three-Group Study to Examine the Efficacy of the Air up® Drinking System at Improving Hydration and Associated Health Outcomes

A

air up

Status

Completed

Conditions

Water Intake

Treatments

Dietary Supplement: Air Up® Orangeade Pod
Dietary Supplement: Air Up® Peach Pod

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

A randomized, controlled trial evaluating the air up® drinking system's impact on hydration and health outcomes. Participants will use air up® with Peach, Orangeade, or unscented pods and their effects on drinking habits, and health outcomes will be assessed over 12 weeks.

Enrollment

50 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Willingness to use the system
  • Generally healthy
  • Enjoys the smell of peach or orangeade.

Exclusion criteria

  • Silicone allergy
  • IBS, bariatric surgery,
  • pregnancy
  • participation in another clinical study.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

50 participants in 3 patient groups

Air Up® Peach Pod
Experimental group
Description:
Participants in this arm will use the air up® drinking system with a peach-flavored pod. The intervention aims to test if the flavored scent encourages increased water intake, which will be assessed by self-reported questionnaires and hydration-related health outcomes over 12 weeks.
Treatment:
Dietary Supplement: Air Up® Peach Pod
Air Up® Orangeade Pod
Experimental group
Description:
Participants in this arm will use the air up® drinking system with an orangeade-flavored pod. Similar to Arm 1, the intervention will assess the impact of the flavored scent on water consumption and health outcomes, using the same methods of evaluation.
Treatment:
Dietary Supplement: Air Up® Orangeade Pod
Control - Unscented Pod
No Intervention group
Description:
Participants in this control arm will use the air up® drinking system with an unscented pod. This group will serve as the control to evaluate the effectiveness of the scented pods in comparison to a baseline with no added scent.

Trial contacts and locations

1

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Central trial contact

Patrick Renner, MSc

Data sourced from clinicaltrials.gov

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