COMPLETED

Impact of Exercise Intervention on Well-being in Shift-working Acute Care Nurses

Conditions

Psychological Wellness exercise whole person health nurses pilot study

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a randomized, wait-list control pilot study to analyze the impact of a 12-week exercise training intervention on post-traumatic growth and whole-person well-being (mental health, physical health, spiritual well-being, perceived social support, and occupational health) among shift-working acute care nurses within AdventHealth.

Official Title

Examining the Impact of a 12-week Worksite Exercise Training Intervention on Mental, Metabolic, Physical, Spiritual, and Occupational Well-being Among Acute Care Nurses: A Randomized, Controlled Mixed Methods Pilot Study

Quick Facts

Study Start:2023-09-13

Study Completion:2025-05-13

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT05966805

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 65 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
Age 18 years or older Willing and able to provide informed consent Able to understand and follow study procedures Stable medical condition	1. Positive urine pregnancy test prior to DEXA scan 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

Inclusion Criteria

Exclusion Criteria

Age 18 years or older
Willing and able to provide informed consent
Able to understand and follow study procedures
Stable medical condition

1. Positive urine pregnancy test prior to DEXA scan
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

Contacts and Locations

Principal Investigator

Andrea Brennan, PhD

PRINCIPAL_INVESTIGATOR

AdventHealth

Study Locations (Sites)

AdventHealth

Orlando, Florida, 32803

United States

Collaborators and Investigators

Sponsor: AdventHealth

Andrea Brennan, PhD, PRINCIPAL_INVESTIGATOR, AdventHealth

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-09-13

Study Completion Date2025-05-13

Study Record Updates

Study Start Date2023-09-13

Study Completion Date2025-05-13

Terms related to this study

Keywords Provided by Researchers

exercise
whole person health
nurses
pilot study

Additional Relevant MeSH Terms

Psychological Wellness