NCT05260840

Brief Summary

The aim of the Fluid at Work Study is to develop and evaluate a fluid intake measurement tool for use in the UK working population. From the results of a systematic review and a round table discussion a novel fluid measurement tool has been developed - the Workplace Beverage Intake Questionnaire (WBIQ) The observational evaluation study will measure the relative validity and reliability of WBIQ for assessing fluid intake in a workplace population.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
71

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 18, 2022

Completed
10 days until next milestone

Study Start

First participant enrolled

February 28, 2022

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 2, 2022

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 20, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2023

Completed
Last Updated

January 25, 2023

Status Verified

February 1, 2022

Enrollment Period

11 months

First QC Date

February 18, 2022

Last Update Submit

January 23, 2023

Conditions

Healthy

Keywords

WorkplaceFluidAssessmentEmployee

Outcome Measures

Primary Outcomes (2)

  • Relative validity of fluid intake measurement

    Measured against 24-hr urine output, specific gravity and 7 day reported fluid intake

    7 days

  • Reliability of fluid intake measurement (l/day)

    Comparison of WBIQ responses at 3 time points

    2 months

Interventions

Evaluation study - provision of an online questionnaireOTHER

Evaluation study - provision of an online questionnaire

Eligibility Criteria

Age19 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Desk based office employees

You may qualify if:

  • Full-time employee working in a desk-based role
  • No history of heart attack, stroke, angina, thrombosis, liver or kidney diseases, diabetes, chronic gastrointestinal disorder, or cancer
  • Able to remain within the UK during the 8-10-week period of testing
  • No history of excess alcohol intake or substance abuse
  • Agree to not drink alcohol for the 7-day period of dietary data collection
  • Not already participating in a clinical trial
  • Not currently taking medication that is likely to alter kidney function or fluid balance
  • Able to understand the information sheet and willing to comply with study protocol
  • Able to give informed written consent

You may not qualify if:

  • Pregnant or breast feeding

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Life Course Sciences

London, SE1 9NH, United Kingdom

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

If participants consent, a urine sample will bio banked for future analyses

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 18, 2022

First Posted

March 2, 2022

Study Start

February 28, 2022

Primary Completion

January 20, 2023

Study Completion

January 20, 2023

Last Updated

January 25, 2023

Record last verified: 2022-02

Locations

GB(1)