Help-Seeking BehaviorNCT05356598
Help-seeking Intentions of ROTC Trainees
A study testing Authority-delivered Health promotion video and Peer-delivered Health Promotion Video in people with Help-Seeking Behavior and Musculoskeletal Injury, run by University of Nevada, Las Vegas.
Trial summary
Online survey measuring pre-post stigma and intentions to seek care for musculoskeletal injuries using peer and authority-delivered health promotion videos. Read more about this study
- Who is it for?
- Ages 18 to 39 yearsHealthy volunteers can take part
- Conditions the study is for
- Help-Seeking Behavior, Musculoskeletal Injury
- What is being tested?
- Authority-delivered Health promotion video and Peer-delivered Health Promotion Video
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 350 participants
- Where
- No sites listed yet
- Study dates
- 1 Sep 2022to 1 Apr 2023
- Phase
- Interventional
- 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 39 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Age 18-39
- Actively participating in a college or university senior ROTC program (Army, Air Force, or Naval)
Who cannot join
- Anyone who does not meet inclusion criteria
Trial locations and contacts
No sites are listed yet.
Kara Radzak, PhD contact
About this study
Official title: Impact of Peer-delivered Versus Authority-delivered Information on Help-seeking Intentions of ROTC Trainees
Online survey measuring pre-post stigma and intentions to seek care for musculoskeletal injuries using peer and authority-delivered health promotion videos.
Read the detailed description
The survey will be hosted via QualtricsXM and accessible via an anonymous link. When participants open the survey, they will be presented with the survey's information sheet explaining the study's purpose and procedures. The information sheet will make it clear that completing the survey is voluntary and cadets may cease the survey at any time. Data from unfinished surveys will not be included in final analyses for any reports produced from this survey. Participants will complete demographics questions. Then, participants will answer injury reporting intentions and stigma questions, presented in a randomized order to reduce respondent fatigue. Participants will then watch a health promotion video that encourages reporting musculoskeletal injuries while in ROTC. Participants have the potential to be shown one of three videos: an officer-delivered health promotion, cadet-delivered health promotion, and a video of an officer exercising. Participants will be randomly assigned to one of the three videos using the in-built randomization function within Qualtrics. After watching the video, participants will answer the stigma and intentions questions again. After, participants will be asked to provide an email address that will be used to send them a link to complete the survey a second time. The follow-up portion will ask for their unique identifier as described above and have the participants answer the stigma and intentions questions again. All data will be de-identified when exporting responses from Qualtrics. No reference will be made to any individual participant in any way when presenting or reporting these data.
- Conditions
- Help-Seeking Behavior, Musculoskeletal Injury
- Being tested
- Authority-delivered Health promotion video, Peer-delivered Health Promotion Video, Control Group Video
- Medical subject headings
- Help-Seeking Behavior
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Authority-delivered Health promotion videoOther
A video delivered by a US Army Lieutenant Colonel (authority figure) encouraging participants to seek help for musculoskeletal injuries experienced while in ROTC.
Peer-delivered Health Promotion VideoOther
A video delivered by a US Army ROTC cadet (peer) encouraging participants to seek help for musculoskeletal injuries experienced while in ROTC.
Control Group VideoOther
Also called Control
Video of a US Army First Lieutenant squatting, bench pressing, and deadlifting with voiceover. No mention of musculoskeletal injuries or help-seeking behavior.
| Study group | Role | What they receive |
|---|---|---|
| Peer-delivered | Experimental | The arm will receive an intervention in the form of a peer-delivered video promoting help-seeking for musculoskeletal injuries while in ROTC. This video will be presented by a current ROTC cadet. Receives: Other: Peer-delivered Health Promotion Video |
| Authority-delivered | Experimental | The arm will receive an intervention in the form of an authority-delivered video promoting help-seeking for musculoskeletal injuries while in ROTC. This video will be presented by a US Army Lieutenant Colonel who is currently a professor of military science for an ROTC battalion. Receives: Other: Authority-delivered Health promotion video |
| Control | Other | The arm will receive no true intervention. Participants in the control arm will watch a video of a US Army First Lieutenant exercising with no reference to musculoskeletal injuries or help-seeking behavior. Receives: Other: Control Group Video |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in Stigma and Help-seeking Intentions Measured Before and After Health Promotion with Three-week Follow-up
Outcome will measure stigma and help-seeking intentions related to musculoskeletal injuries using an online survey. Survey items use a seven-point Likert scale where the most positive response is assigned the lowest number (1) while the most negative response is assigned the highest number (7).
Measured: Three weeks (baseline, immediately post intervention, and three weeks post intervention)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 May 2022
- Study start1 Sep 2022 (estimated)
- Primary completion15 Dec 2022 (estimated)
- Study completion1 Apr 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Help-Seeking BehaviorStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 350 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Nevada, Las Vegas
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Kara Radzak, PhD, Principal investigator, University of Nevada, Las Vegas
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05356598
- Sponsor's protocol ID
- UNLV-2022-55
- Status last verified
- Apr 2022
- First submitted
- 26 Apr 2022
- Last updated
- 5 May 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 5 May 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Peer-delivered Versus Authority-delivered Information on Help-seeking Intentions of ROTC Trainees
- ClinicalTrials.gov ID
- NCT05356598
- Acronym / sponsor ID
- UNLV-2022-55
- Conditions
- Help-Seeking Behavior, Musculoskeletal Injury
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 350 participants (estimated)
- Lead sponsor
- University of Nevada, Las VegasUniversity, hospital or other
- Study start
- 1 Sep 2022 (estimated)
- Primary completion
- 15 Dec 2022 (estimated)
- Study completion
- 1 Apr 2023 (estimated)
- First posted
- 2 May 2022 (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.
Online survey measuring pre-post stigma and intentions to seek care for musculoskeletal injuries using peer and authority-delivered health promotion videos.
Detailed description
The survey will be hosted via QualtricsXM and accessible via an anonymous link. When participants open the survey, they will be presented with the survey's information sheet explaining the study's purpose and procedures. The information sheet will make it clear that completing the survey is voluntary and cadets may cease the survey at any time. Data from unfinished surveys will not be included in final analyses for any reports produced from this survey. Participants will complete demographics questions. Then, participants will answer injury reporting intentions and stigma questions, presented in a randomized order to reduce respondent fatigue. Participants will then watch a health promotion video that encourages reporting musculoskeletal injuries while in ROTC. Participants have the potential to be shown one of three videos: an officer-delivered health promotion, cadet-delivered health promotion, and a video of an officer exercising. Participants will be randomly assigned to one of the three videos using the in-built randomization function within Qualtrics. After watching the video, participants will answer the stigma and intentions questions again. After, participants will be asked to provide an email address that will be used to send them a link to complete the survey a second time. The follow-up portion will ask for their unique identifier as described above and have the participants answer the stigma and intentions questions again. All data will be de-identified when exporting responses from Qualtrics. No reference will be made to any individual participant in any way when presenting or reporting these data.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Peer-delivered | Experimental | Other: Peer-delivered Health Promotion VideoThe arm will receive an intervention in the form of a peer-delivered video promoting help-seeking for musculoskeletal injuries while in ROTC. This video will be presented by a current ROTC cadet. |
| Authority-delivered | Experimental | Other: Authority-delivered Health promotion videoThe arm will receive an intervention in the form of an authority-delivered video promoting help-seeking for musculoskeletal injuries while in ROTC. This video will be presented by a US Army Lieutenant Colonel who is currently a professor of military science for an ROTC battalion. |
| Control | Other | Other: Control Group VideoThe arm will receive no true intervention. Participants in the control arm will watch a video of a US Army First Lieutenant exercising with no reference to musculoskeletal injuries or help-seeking behavior. |
Who may qualify
- Ages
- 18 to 39 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Age 18-39
- Actively participating in a college or university senior ROTC program (Army, Air Force, or Naval)
Key exclusion criteria (1 listed)
- Anyone who does not meet inclusion criteria
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 |
|---|---|---|
| Authority-delivered Health promotion videoA video delivered by a US Army Lieutenant Colonel (authority figure) encouraging participants to seek help for musculoskeletal injuries experienced while in ROTC. | Other | Authority-delivered |
| Peer-delivered Health Promotion VideoA video delivered by a US Army ROTC cadet (peer) encouraging participants to seek help for musculoskeletal injuries experienced while in ROTC. | Other | Peer-delivered |
| Control Group VideoAlso: ControlVideo of a US Army First Lieutenant squatting, bench pressing, and deadlifting with voiceover. No mention of musculoskeletal injuries or help-seeking behavior. | Other | Control |
Primary outcome
Changes in Stigma and Help-seeking Intentions Measured Before and After Health Promotion with Three-week Follow-up
Time frame: Three weeks (baseline, immediately post intervention, and three weeks post intervention)
Outcome will measure stigma and help-seeking intentions related to musculoskeletal injuries using an online survey. Survey items use a seven-point Likert scale where the most positive response is assigned the lowest number (1) while the most negative response is assigned the highest number (7).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 May 2022.
- Individual participant dataSharing planned: Undecided
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Mental Health Help-seeking Promotion in Older Adults
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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.
Kara Radzak, PhD contact
Kara Radzak, PhD principal investigator
University of Nevada, Las Vegas
Questions about this trial
What is this clinical trial studying?
A study testing Authority-delivered Health promotion video and Peer-delivered Health Promotion Video in people with Help-Seeking Behavior and Musculoskeletal Injury, run by University of Nevada, Las Vegas.
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 1 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: status not confirmed, as of the sponsor's last update on 5 May 2022. Status can change between updates, so confirm with the study contact before making plans.
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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Joshua D Wooldridge, MS (5852016220, joshua.wooldridge@unlv.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in Stigma and Help-seeking Intentions Measured Before and After Health Promotion with Three-week Follow-up (time frame: Three weeks (baseline, immediately post intervention, and three weeks post intervention)). 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 5 May 2022.