- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06878157
Ontological Coaching Among Nurses (OCN) (OCN)
Ontological Coaching Among Novice Nurses (OCN): a Mixed Methods Study
This study aims to develop and evaluate ontological coaching among novice nurses in Singapore. The specific aims of this project are: (1) to develop theory based Ontological Coaching among Nurses (OCN) intervention for novice nurses; (2) examine its effectiveness on nurses' psychological wellbeing (primary outcome), help-seeking behavior (social support), goal setting, resilience, intention to leave and job satisfaction (Secondary outcomes); and (3) examine the perceptions of nurses in receiving this intervention.
The specific research questions we plan to answer in this project are:
- How the OCN will influence psychological wellbeing of the new nurses?
- How the OCN will enhance the new nurses social support and goal setting for their reality and future?
- How the OCN will influence new nurses' resilience, intention to leave and job satisfaction?
- What are the changes in psychological well-being, social support, goal setting, resilience, intention to leave and job satisfaction after receiving OCN over time (pre-test and post-test)?
- Are there any strengths, weaknesses and area of improvements (overall experience) for the use of OCN among new nurses?
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Singapore, Singapore
- National University Hospital
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Singapore, Singapore
- Ng Teng Fong General Hospital
-
Singapore, Singapore
- Alexandra Hospital
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Singapore, Singapore
- National University Polyclinics
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Nurses:
- 21 years old and above
- are able to read and speak English,
- have 0-10 years of working experience after the registration with Singapore Nursing Board (SNB)
- currently working at the study venues with the valid registered nurse license with the SNB
- who are willing to be audio-recorded if invited for an interview
Facilitators:
- who hold an Ontological Coaching certification and a minimum of 50 hours of Coaching experience
Exclusion Criteria:
Nurses:
- have physical or mental disorders which would interfere with their ability to participate in the study
- have refused to participate in this study
Facilitators:
- who does not hold an Ontological Coaching certification or who do not have a minimum of 50 hours of Coaching experience
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Coaching
In the form of small groups (3-6 participants), the nurses will receive a knowledge based session (maximum 1 hour long) to share about ontological coaching.
After the group session, each nurse will receive 4 individual sessions (30-60 minutes) on monthly basis.
|
Group session: This session will provide an overview of coaching and the following topics will be covered: 1) Experience coaching in teams, 2) The Ideal Life, 3) The Coaching Distinction, 4) Introduction to Body, Emotions, Language (BEL), 5) Deeper understanding of BEL, 6) Applying BEL to clinical scenarios, 7) The coaching perspective in Nursing, 8) Re-visit the Ideal Life, 9) Explore mental/emotional/physical challenges in practicing nursing, 10) Time and stress management, work-life balance; Individual Session: This individualized session will cover the discussions on the topic brought up by novice nurses.
The aim of this session is to: 1) Help novice nurses design the steps in their journey towards what they care about, 2) Explore the nurses' world by asking encouraging and evoking questions, 3) Collaborate with nurses in a stimulating and imaginative manner that help them to optimize their potential, 4) Co-create with nurses the professional and personal identity they strive for
|
|
No Intervention: Conotrol
Participants do not undergo any ontological coaching.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effectiveness on nurses' psychological wellbeing
Time Frame: baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
Ryff Scales of Psychological Well-Being: a 42-item instrument Psychological Wellbeing (PWB) Scale measures six aspects of wellbeing and happiness: autonomy, environmental mastery, personal growth, positive relations with others, purpose in life, and self-acceptance.
Respondents rate how strongly they agree or disagree with 42 statements using a 7-point scale (1 = strongly agree; 7 = strongly disagree).
|
baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress
Time Frame: baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
Nursing Stress Scale: a 34-item instrument that describe situations that have been identified as causing stress for nurses in the performance of their duties.
Respondents how strongly they agree or disagree with 34 statements using a 4-point scale (1 = never; 4 = very frequently).
|
baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
|
Help-seeking behavior (social support)
Time Frame: baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
Sarason's social support questionnaire - short form (SSQSR): a 6-item instrument to evaluate the availability and satisfaction associated with an individual's social support systems.
Respondents indicate the number of people available to provide support in 6 areas and then rate the overall level of satisfaction with the support given in each of the areas using a 6-point scale (1 = very dissatisfied; 6 = very satisfied).
|
baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
|
Goal Setting
Time Frame: baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
Goal Setting Questionnaire (GSQ): an 18-item instrument to evaluate individuals' competencies in three areas: setting meaningful goals, focusing on personal improvement, and incorporating prior experiences, interests, skills, and feedback from family, peers, or a trusted individual.
Respondents rate how strongly they agree or disagree with 18 statements using a 5-point scale (1 = not very like me; 5 = very like me)
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baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
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Intention to Leave
Time Frame: baseline, 2-3 months (intervention), 4-6 months (post intervention)
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Roodt's turnover scale (TIS-6): a 6-item instrument to measure turnover intention.
Respondents rate how strongly they agree or disagree with 6 statements using a 5-point scale (1 = never; 5 = always)
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baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
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Job Satisfaction
Time Frame: baseline, 2-3 months (intervention), 4-6 months (post intervention)
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Bowling Green State University's The Job Satisfaction Scale: measures employee attitudes such as job satisfaction.
Respondents indicate their satisfaction in 5 areas (Y = Yes; N = No; ?
= Cannot Decide).
|
baseline, 2-3 months (intervention), 4-6 months (post intervention)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Shefaly Shorey, PhD, National University of Singapore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NHG DSRB 2022/00676
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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