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

5. august 2026 oppdatert av: Bounce Curl

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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

40

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Nevada
      • Las Vegas, Nevada, Forente stater, 89101
        • Citruslabs

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Bounce Curl Conditioning Mask
All 40 participants receive the Bounce Curl conditioning mask and apply it twice per week over one week. After shampooing, participants apply a generous amount from ends to roots, leaving it on for 1 minute at the first application and 5 minutes at the second application.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Self-Reported Hair Health
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair health assessed via self-reported questionnaire
Baseline, after first use, and Week 1

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Self-Reported Hair Quality
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair quality assessed via self-reported questionnaire
Baseline, after first use, and Week 1
Change in Self-Reported Hair Breakage
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair breakage assessed via self-reported questionnaire
Baseline, after first use, and Week 1
Change in Self-Reported Hair Hydration
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair hydration assessed via self-reported questionnaire
Baseline, after first use, and Week 1
Change in Self-Reported Hair Detangling
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair detangling assessed via self-reported questionnaire
Baseline, after first use, and Week 1
Change in Self-Reported Hair Softness
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair softness assessed via self-reported questionnaire
Baseline, after first use, and Week 1
Change in Self-Reported Hair Frizz
Tidsramme: Baseline, after first use, and Week 1
Mean change in participant-reported hair frizz assessed via self-reported questionnaire
Baseline, after first use, and Week 1

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. januar 2026

Primær fullføring (Faktiske)

1. april 2026

Studiet fullført (Faktiske)

1. april 2026

Datoer for studieregistrering

Først innsendt

5. august 2026

Først innsendt som oppfylte QC-kriteriene

5. august 2026

Først lagt ut (Faktiske)

10. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

5. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 20779
  • legacy-20779

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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