- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03448224
Behavioral Intervention in Reducing Indoor Tanning
The Development and Evaluation of a Behavioral Intervention to Reduce Indoor Tanning
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
PRIMARY OBJECTIVE:
To develop and evaluate an online tailored indoor tanning (IT) intervention based on findings from phase 1.
OUTLINE:
INTERVENTION: Participants are randomized to 1 of 2 groups.
GROUP I: Participants receive intervention, weekly text messages about IT reduction, and personalized booster intervention. Participants then receive text messages twice weekly for 4 weeks.
GROUP II: Participants are placed on wait-list and may receive full intervention after follow-up.
After completion of study, patients are followed up at 3 months.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Kentucky
-
Lexington, Kentucky, Forenede Stater, 40536
- University of Kentucky
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Use of IT at least 25 times in the past year
- Women
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Group I (web-based Indoor Tanning intervention)
Participants receive intervention, weekly text messages about IT reduction, and personalized booster intervention.
Participants then receive text messages twice weekly for 4 weeks.
|
Questionnaire
Intervention
|
Aktiv komparator: Group II (wait-list)
Participants are placed on wait-list and may receive full intervention after follow-up.
|
Questionnaire
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Number of Prior 2-Month Indoor Tanning Sessions Reported by Participants on a Follow-up Survey
Tidsramme: Up to 3 months
|
On the follow-up assessment administered 3 months after the baseline assessment, participants will estimate the number of times they used a tanning bed or booth with tanning lamps in the past 2 months with an open-ended response.
|
Up to 3 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Perceived Difficulty (Self-efficacy) in Quitting Tanning
Tidsramme: At 3 months post-intervention
|
Measured at post-intervention data collection (3 months post intervention) using single item assessment: "How hard would it be for you to stop using tanning beds/booths?"
(Please answer on a scale for 0-10, where 0 is "Not at all hard", 10 is "Extremely hard").
|
At 3 months post-intervention
|
Sunburns
Tidsramme: Up to 3 months
|
On the follow-up assessment administered 3 months after the baseline assessment, participants will estimate the number of times they had a sunburn in the past 2 months with an open-ended response.
|
Up to 3 months
|
Intentions to Use Indoor Tanning
Tidsramme: Up to 3 months
|
For tanning intentions, participants indicated how likely they were to use an indoor tanning bed in the next year on a 6-point response scale anchored with 1 = Extremely unlikely and 6 = Extremely likely
|
Up to 3 months
|
Number of Participants Expressing Positive Interest in Changing Tanning
Tidsramme: 3 months
|
Interest in changing tanning was assessed using a single item: Would you like to reduce or quit indoor tanning if you could do so easily?
Responses coded as 0 = no and 1 = yes
|
3 months
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 131315 (Anden identifikator: Rutgers Cancer Institute of New Jersey)
- P30CA072720 (U.S. NIH-bevilling/kontrakt)
- NCI-2018-00063 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- Pro2013003349 (Anden identifikator: Rutgers Cancer Institute of New Jersey)
- K07CA175115 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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