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Worksite Wellness Program for Occupational Stress (WHHIP-PLUS Trial)
N/A
Waitlist Available
Led By Kelly Doran, PhD, RN
Research Sponsored by University of Maryland, Baltimore
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Staff: Passed the evaluation to sign consent
Resident: 55 years or older
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 6-months, 12-months
Awards & highlights
WHHIP-PLUS Trial Summary
This trial will test if a worksite wellness program can help reduce worker stress and improve cardiovascular disease among long-term care workers.
Who is the study for?
This trial is for English-speaking staff aged 18+ working in long-term care facilities and residents aged 55+, who can also understand English. Participants must be able to consent to the study. It aims to help those experiencing job stress and looking to reduce lifestyle risks for cardiovascular disease.Check my eligibility
What is being tested?
The study is testing a worksite wellness program called WHHIP PLUS, designed to lower stress and improve heart health among healthcare workers. The effectiveness of this program will be compared with an education-only approach.See study design
What are the potential side effects?
Since this trial involves a wellness program rather than medication, side effects are not typical as with drug trials. However, participants may experience changes in their routine that could affect their daily habits or cause temporary discomfort.
WHHIP-PLUS Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am authorized to give consent.
Select...
I am 55 years old or older.
Select...
I can understand and speak English.
Select...
I am 18 years old or older.
WHHIP-PLUS Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 6-months, 12-months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6-months, 12-months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Cardiovascular disease risk
Secondary outcome measures
Job strain model tool
Short version of the Depression Anxiety Stress Scale-Stress- (DASS-S)
Other outcome measures
3 word recall from mini-cog
Barthel index
Bioelectrical Impedance Analysis (BIA)
+5 moreWHHIP-PLUS Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: WHHIP-PLUS and Function Focused CareExperimental Treatment1 Intervention
Component I: Stakeholder Group Involvement:
Component II: Environment Assessment:
Component III: Organizational Changes To Reduce Job Stress:
Component IV- Worker Health Behavior Change including function focused care interventions
Group II: Education onlyActive Control1 Intervention
Education
Find a Location
Who is running the clinical trial?
University of Maryland, BaltimoreLead Sponsor
687 Previous Clinical Trials
374,171 Total Patients Enrolled
University of Maryland, School of NursingUNKNOWN
American Heart AssociationOTHER
324 Previous Clinical Trials
4,933,303 Total Patients Enrolled
2 Trials studying Occupational Stress
450 Patients Enrolled for Occupational Stress
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am over 18, speak English, work here, and can legally consent.I am authorized to give consent.I am 55 years old or older.I am considered capable of understanding and signing the consent form.I am 55 or older, speak English, live in the facility, and can legally consent.I can understand and speak English.I am 18 years old or older.
Research Study Groups:
This trial has the following groups:- Group 1: Education only
- Group 2: WHHIP-PLUS and Function Focused Care
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
To what extent has the number of individuals enrolled in this clinical trial been limited?
"That is accurate. Clinicaltrials.gov divulges that this medical investigation, which was first advertised on June 28th 2022, is presently recruiting individuals for participation. In total, 564 patients are required to be recruited from a single clinical center."
Answered by AI
Are recruitment efforts underway for this research study?
"According to clinicaltrials.gov, this scientific experiment is presently enrolling participants - it has been available since June 28th 2022 and was recently amended on September 6th 2022."
Answered by AI
Who else is applying?
What site did they apply to?
Edenwald Senior Living
What portion of applicants met pre-screening criteria?
Met criteria
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