A Clinical Trial to Evaluate the Effects of a Conditioning Mask on Hair Health, Breakage, Hydration, and Detangling

Bounce Curl

Status

Completed

Conditions

Hair Health

Hair Detangling

Hair Hydration

Hair Frizz

Hair Breakage

Treatments

Dietary Supplement: Bounce Curl Conditioning Mask

Study type

Interventional

Funder types

Industry

Identifiers

NCT07755865

20779

legacy-20779

Details and patient eligibility

About

This study evaluates the effects of the Bounce Curl conditioning mask on hair health, breakage, hydration, and detangling. The trial is conducted as a single-arm, unblinded, virtual study in which all 40 enrolled participants use the test product twice per week over a one-week period.

Participants complete self-reported questionnaires at Baseline, after the first use, and at the end of Week 1. The primary objective is to examine the product's effects on hair health as reported by participants, while secondary objectives assess perceived changes in hair quality, hydration, breakage, detangling, softness, and frizz.

Enrollment

40 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Be male or female.
Be aged 18-50.
Must have self-reported curly, coily, or wavy hair.
In the past four weeks, has been experiencing issues regarding all of the following: hair health, hair breakage, hair hydration, and hair tangling.
Anyone who washes and styles their hair at least once per week.
Anyone who has been using the same hair care routine and products for at least one month prior to the study and is willing to maintain this for the study duration, i.e. shampoo and styling products.
If taking any vitamins, minerals, or herbal supplements that target hair health, has been doing so for at least three months and is willing to maintain this routine for the duration of the study.
Willing to avoid introducing any new products or any forms of medications or supplements that target hair health and appearance during the study period.
Willing to avoid any chemical treatments to the hair during the study period, e.g. chemical straightening, hair extensions with chemical bonding, perms, and relaxers.
Willing to avoid any form of protective styles (braids, singles, corn rows, etc) during the study period.
Anyone willing to refrain from dying, highlighting, or cutting their hair for the study duration.
Resides in the United States.
Anyone who considers themselves in general good health.

Exclusion criteria

Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological, psychiatric disorders, and history of illness in the last three months.
Anyone who has gotten a hair chemical treatment (e.g., keratin, dyeing, bleaching, perms) in the last month.
Is currently undergoing or planning to undergo any significant medical procedures during the study period.
Currently taking any prescription medication for hair loss.
Currently has hair in any protective styles such as braids, cornrows, or singles.
Anyone with any conditions that affect the hair or scalp (e.g., alopecia areata).
Anyone with any allergies or sensitivities to any of the study product ingredients.
Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period).
Anyone unwilling to follow the study protocol.
Anyone with a history of substance abuse.