Health Status UnknownNCT04179227
Focus Group in Collecting Feedbacks From Indoor Tanning Bed Users for Social Media-Delivered Intervention Development
An observational study of Health Status Unknown, run by Rutgers, The State University of New Jersey at 1 site in United States.
Trial summary
This research trial collects feedbacks from indoor tanning bed users via focus group for the development of social media-delivered intervention. Conducting a focus group with people using indoor tanning bed and having access to Facebook may help doctors to better understand people's perspective and thoughts about the… Read more about this study
- Who is it for?
- Ages 18 to 25 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Health Status Unknown
- What is being tested?
- Questionnaire Administration and Survey Administration
- How many people
- 20 participants
- Where
- 1 siteUnited States
- Study dates
- 13 Mar 2017to 6 Sep 2020
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 25 years
- Women only
- Healthy volunteers accepted
- Adult
Study population: Facebook users use of an indoor tanning bed at least 10 times in the past 12 months
Who may be able to join
- Use of an indoor tanning bed at least 10 times in the past 12 months
- At least daily use of Facebook
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
United States1 site
Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, 08903
About this study
Official title: Developing a Social Media-Delivered Intervention
This research trial collects feedbacks from indoor tanning bed users via focus group for the development of social media-delivered intervention. Conducting a focus group with people using indoor tanning bed and having access to Facebook may help doctors to better understand people's perspective and thoughts about the various Facebook messages.
Read the detailed description
PRIMARY OBJECTIVES:
- To elicit feedback from young adult women who use indoor tanning beds on preliminary intervention content.
OUTLINE:
Participants attend a focus group session and review printed copies of planned posts for the to-be-developed Facebook intervention over 90 minutes to 2 hours.
- Conditions
- Health Status Unknown
- Being tested
- Questionnaire Administration, Survey Administration
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Questionnaire AdministrationOther
Ancillary studies
Survey AdministrationOther
Ancillary studies
| Study group | Role | What they receive |
|---|---|---|
| Observational (focus group) | Participants attend a focus group session and review printed copies of planned posts for the to-be-developed Facebook intervention over 90 minutes to 2 hours. Receives: Other: Questionnaire Administration; Other: Survey Administration |
What is being measured
The primary outcome is the main question the study is designed to answer.
Participants feedback
Focus group questions will elicit descriptions of general interest. Participants will also rate various posts on the hand-out sheets included in the script.
Measured: Up to 2 years
Participants feedback
Focus group questions will elicit descriptions of posts, and as well as suggestions for improving existing posts or creating new ones. Participants will also rate various posts on the hand-out sheets included in the script.
Measured: Up to 2 years
Participants feedback
Focus group questions will elicit descriptions of general interest of topics. Participants will also rate various posts on the hand-out sheets included in the script.
Measured: Up to 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Nov 2019
- Study start13 Mar 2017
- Primary completion21 Apr 2018
- Study completion6 Sep 2020
Why it stopped: PI left institution.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Health Status UnknownStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Ecologic or community
- Time perspective
- Prospective
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- Rutgers, The State University of New Jersey
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Responsible party
- Principal investigator, Sharon Manne, PhD, Rutgers Cancer Institute of New Jersey
- Investigators
- Sharon Manne, Principal investigator, Rutgers Cancer Institute of New Jersey
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04179227
- Sponsor's protocol ID
- Pro20170000136
- Other IDs
- NCI-2018-00058, Pro20170000136, 131703, P30CA072720
- Status last verified
- Apr 2021
- First submitted
- 25 Nov 2019
- Last updated
- 8 Apr 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Apr 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Developing a Social Media-Delivered Intervention
- ClinicalTrials.gov ID
- NCT04179227
- Acronym / sponsor ID
- Pro20170000136
- Conditions
- Health Status Unknown
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: PI left institution.
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Rutgers, The State University of New JerseyUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Study start
- 13 Mar 2017 (actual)
- Primary completion
- 21 Apr 2018 (actual)
- Study completion
- 6 Sep 2020 (actual)
- First posted
- 27 Nov 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This research trial collects feedbacks from indoor tanning bed users via focus group for the development of social media-delivered intervention. Conducting a focus group with people using indoor tanning bed and having access to Facebook may help doctors to better understand people's perspective and thoughts about the various Facebook messages.
Detailed description
PRIMARY OBJECTIVES:
- To elicit feedback from young adult women who use indoor tanning beds on preliminary intervention content.
OUTLINE:
Participants attend a focus group session and review printed copies of planned posts for the to-be-developed Facebook intervention over 90 minutes to 2 hours.
Study design
- Observational model
- Ecologic or community
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Observational (focus group) | – | Other: Questionnaire Administration, Other: Survey AdministrationParticipants attend a focus group session and review printed copies of planned posts for the to-be-developed Facebook intervention over 90 minutes to 2 hours. |
Who may qualify
- Ages
- 18 to 25 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Facebook users use of an indoor tanning bed at least 10 times in the past 12 months
Key inclusion criteria (2 listed)
- Use of an indoor tanning bed at least 10 times in the past 12 months
- At least daily use of Facebook
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Questionnaire AdministrationAncillary studies | Other | Observational (focus group) |
| Survey AdministrationAncillary studies | Other | Observational (focus group) |
Primary outcome
Participants feedback
Time frame: Up to 2 years
Focus group questions will elicit descriptions of general interest. Participants will also rate various posts on the hand-out sheets included in the script.
Participants feedback
Time frame: Up to 2 years
Focus group questions will elicit descriptions of posts, and as well as suggestions for improving existing posts or creating new ones. Participants will also rate various posts on the hand-out sheets included in the script.
Participants feedback
Time frame: Up to 2 years
Focus group questions will elicit descriptions of general interest of topics. Participants will also rate various posts on the hand-out sheets included in the script.
Results and safety
The study was stopped early (reason given: PI left institution.). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Apr 2021.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sharon Manne principal investigator
Rutgers Cancer Institute of New Jersey
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Health Status Unknown, run by Rutgers, The State University of New Jersey at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 8 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: PI left institution.). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Participants feedback (time frame: Up to 2 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Apr 2021.