STUDY ANNOUNCEMENT
Ageratum Grey Hair Study
Do you have greying hair?
Seeking generally healthy adults over 18 years who have light to moderate mixed grey hair at their temples to help assess a herbal hair serum on grey hair density and appearance.
Thank you for your interest in our grey hair study, which is investigating the effects of Ageratum conyzoides, a subtropical herb, on reducing grey hair density and appearance.
Please note: This page is a summary of the study outline and participant requirements. A full Participant Information Sheet with more detailed information will be provided to you before you are asked to give your consent to participate.
How long is the study, and when does it start?
Your involvement in this study will be required for 12 weeks. We are recruiting on a rolling basis which means that your individual start date is flexible.
Please see below for more information. You can find the eligibility and registration form at the bottom of this page.
About the product you’ll help investigate…
This study is assessing the effectiveness of a topical hair serum containing Ageratum.
Ageratum is a sub-tropical herb, traditionally used for its medicinal properties on a wide range of conditions including wound healing and other skin related complaints.
The hair serum is applied to your entire scalp, twice daily, morning and night.
As this is an open label study, all participants will be on the active treatment, Ageratum serum.
Why is this study being conducted?
Recent research on Ageratum conyzoides showed positive effects on hair health and it’s possible that the plant biochemicals found in Ageratum may reduce grey hair density and appearance.
What is required of participants?
Your involvement in the study will be for 12 weeks. Some of the study requirements can be completed online at home, however, you will be required to attend four clinic visits at Week 0, Week 4, Week 8, and Week 12.
At each clinic visit you will complete a range of assessments including height, weight, blood pressure, pulse rate, grey hair density and percentage assessments and a short questionnaire. Photographs of your scalp will be taken as part of the assessments. You will also be required to apply the topical hair serum morning and night for 12 weeks.
The information we collect during the study will enable the investigators to assess the hair serum’s effectiveness.
To make the timings of these visits as convenient as possible for you, we are recruiting on a rolling basis. This means that your individual start date is flexible. The RDC Clinic is open 6 days a week (from 6.30am).
Please note: This page is a summary of the study outline and participant requirements. A full Participant Information Sheet with detailed information will be provided to you before you are asked to give your consent to participate.
Payment
You will be eligible for a reimbursement for your time. The payment will be made via direct deposit to your nominated bank account once all study requirements have been met.
If you would like to participate, we’d love to hear from you. Please register your interest by answering the questionnaire and completing the form on this page…we’ll then get in touch to screen you for eligibility.
Study Location
Our clinic is located on Level 3, 252 St Pauls Terrace, Fortitude Valley.
We have free undercover parking for participants directly next door under the Kennigo Hotel, 22 Kennigo Street, Fortitude Valley.
Getting to Us
- Private Transport: free undercover parking available at Kennigo Hotel Car Park
- Train: Fortitude Valley Train Station (350m away)
- Bus: multiple bus stops within close proximity
Check if you can register to take part…
- Adults over 18 years of age
- Generally healthy with no uncontrolled or serious illnesses
- Have a light to moderate mix of grey hair in the temple region
- Able to provide informed consent
- Able to commit to completing the study requirements
Please register your interest by answering the questionnaire and completing the form on this page… we’ll then get in touch to screen you for suitability.
A full Participant Information Sheet with more detailed information will be provided to you before you are asked to give your consent to participate.
Ethics approval and privacy
This RDC Clinical study has been approved by the Bellberry Human Research Ethics Committee under Approval Number: (insert number). The study is also registered on the clinicaltrials.gov under Registration Number: (insert number).
Trained trial coordinators will supervise your progress throughout the study. Your results will be made available to you at the conclusion of the study. Any of your personal information collected during the study will be kept in the strictest confidence.