A Single Group Study to Evaluate the Effects of a Multivitamin on a Range of Health and Wellbeing Outcomes.

NCT ID: NCT06568146

Last Updated: 2024-10-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-23

Study Completion Date

2024-10-23

Brief Summary

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This is a hybrid single-group clinical trial that will last 12 weeks. Participants will take 2 capsules daily with the first meal of the day in the morning. Participants will undertake blood tests at Baseline and Week 12. Study-specific questionnaires will be completed at Baseline, Week 4, Week 8, and Week 12. Cognitive Battery Testing will take place at Baseline, Week 4, Week 8, and Week 12.

Detailed Description

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Conditions

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Health and Wellbeing

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

This is a hybrid single-group clinical trial designed to evaluate the effects of a multivitamin on a range of health and wellbeing outcomes over a 12-week period.
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

This is an open-label study where no masking will be implemented.

Study Groups

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Multivitamin Supplement Group

Participants in this arm will take 2 capsules of the multivitamin supplement daily with the first meal of the day in the morning.

Group Type EXPERIMENTAL

Multivitamin Supplement

Intervention Type DIETARY_SUPPLEMENT

: Participants will take 2 capsules of the multivitamin supplement daily with the first meal of the day in the morning.

Interventions

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Multivitamin Supplement

: Participants will take 2 capsules of the multivitamin supplement daily with the first meal of the day in the morning.

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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Daily Love Multivitamin

Eligibility Criteria

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Inclusion Criteria

* Female at birth.
* Aged 18+.
* Interested in supporting their health and wellbeing.
* Not planning to introduce or change prescription medications, vitamins, minerals, or supplements one month prior to and during the study.
* Generally healthy with no uncontrolled chronic conditions.

Exclusion Criteria

* Recent surgeries or invasive treatments.
* Introduction of new health-related products in the last 12 weeks.
* Allergies to product ingredients or use of Epi-Pen.
* Chronic health conditions affecting participation.
* Endocrine or glucose-related disorders, including diabetes.
* Hematological disorders, including anemia.
* Pregnant, breastfeeding, or planning to conceive.
* History of substance abuse or recent smoking.
* Unwillingness to follow the study protocol.
* Participation in other clinical trials.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Citruslabs

INDUSTRY

Sponsor Role collaborator

Love Wellness

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Citruslabs

Santa Monica, California, United States

Site Status

Countries

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United States

Other Identifiers

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20432

Identifier Type: -

Identifier Source: org_study_id

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