Impact of Exercise Intervention on Well-being in Shift-working Acute Care Nurses
NCT ID: NCT05966805
Last Updated: 2025-11-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
21 participants
INTERVENTIONAL
2023-09-13
2025-05-13
Brief Summary
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Detailed Description
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Phase I (90 minutes): This phase consists of reviewing and obtaining consent, screening for inclusion/exclusion criteria, reviewing study details, and assessing the need for medical clearance to participate in the exercise intervention, and a single blood draw for fasted blood profiles.
Phase II (7 hours): Upon successful screening, all participants will complete baseline assessments.
Phase III (Exercise Training Group 34 hours/Wait-List Control 4.5 hours): Upon completion of Phase II, participants will be randomized to the exercise training intervention group or the wait-list control group.
Phase IV (7 hours): All participants will enter a post-intervention phase that includes repeat assessments of Phase II outcomes.
Phase V (\~2 hours): A subset of psychometric questionnaires will be repeated 3- and 6-months post-exercise training intervention to ascertain sustainability of the intervention.
\*Subjects randomized to the wait-list control group will be offered the exercise training intervention upon completion of the Phase V assessments.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Exercise Training Group
Exercise intervention group will undergo a 12-week exercise program.
Exercise training group
12-Week Exercise intervention on mentaL, metabolic, physicaL, spiritual, social, and occupational well-being among shift-working acute care NURSE
Wait-List Control Group
Wait-List control group will participate in visits every 4 weeks for data collection and periodic phone calls for monitoring. They will be offered the exercise training intervention option at conclusion.
Wait-List Control Group
Control group
Interventions
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Exercise training group
12-Week Exercise intervention on mentaL, metabolic, physicaL, spiritual, social, and occupational well-being among shift-working acute care NURSE
Wait-List Control Group
Control group
Eligibility Criteria
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Inclusion Criteria
2. Nurse working in an AdventHealth inpatient acute care setting
3. Currently working as a shift-working acute care nurse within AdventHealth.
4. Weight stable prior to beginning the study exercise training intervention.
5. Able to speak and understand written and spoken English.
6. Understands the procedures and agrees to participate by giving written informed consent.
7. Willing and able to comply with scheduled visits, laboratory tests, and other study procedures including a 12-week exercise training program.
Exclusion Criteria
2. Uncontrolled Type 1 or Type 2 diabetes mellitus
3. Bleeding disorders
4. Acute or chronic infections
5. Chronic obstructive pulmonary disease
6. Renal insufficiency or nephritis
7. Uncontrolled hypertension (BP\>160 mmHg systolic or \>100 mmHg diastolic)
8. History of Cushing's disease or syndrome
9. Active rheumatoid arthritis or other inflammatory rheumatic disorder
10. Major surgery within 4 weeks prior to Screening
11. Participation in studies involving investigational drug(s) within 30 days prior to Screening
12. History or presence of cardiovascular disease (unstable angina, myocardial infarction or coronary revascularization within 6 months, presence of cardiac pacemaker, implanted cardiac defibrillator)
13. Any malignancy not considered cured, except basal cell carcinoma and squamous cell carcinoma of the skin (a participant is considered cured if there has been no evidence of cancer recurrence in the previous 5 years)
14. Presence of any condition that, in the opinion of the Investigator or medical investigator, compromises participant safety or data integrity or the participant's ability to complete study days.
15. More than 1-day a week of intentional exercise
16. Medically diagnosed sleep disorder
17. Weight \>450 lbs
21 Years
65 Years
ALL
Yes
Sponsors
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AdventHealth
OTHER
Responsible Party
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Principal Investigators
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Andrea Brennan, PhD
Role: PRINCIPAL_INVESTIGATOR
AdventHealth
Locations
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AdventHealth
Orlando, Florida, United States
Countries
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References
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Other Identifiers
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1762353
Identifier Type: -
Identifier Source: org_study_id