Family Supportive Supervisor Training and Workplace Assessment Tool (FSST)

September 24, 2024 updated by: Ellen Ernst Kossek, Work Life Help
This study will evaluate the effectiveness of FSST 2.0 (family supportive supervisor training plus support for use of family and sick leaves) using a randomized control trial design. We expect the intervention will increase supervisors' family supportive and leave supportive behaviors, which in turn will increase employees' leave use and decrease employees' work-family conflict, emotional exhaustion, depressive symptoms, and turnover intentions. This study will enroll a minimum 200 groups of managers and their employees. Managers in the intervention condition will complete pre- and 2 post-intervention Workplace Assessments, 2 online training modules, 1 webinar where managers can review intervention content and ask questions and share reactions on the materials. Managers in the control group and employees in both groups will complete pre- and 2 post-intervention Workplace Assessments. The post-intervention Workplace Assessment will be completed 3 and 6 months after the intervention. The total duration of the study is 9 months as the wait list control group will be offered the intervention and 2nd follow up survey after the 6-month trial.

Study Overview

Detailed Description

This study will evaluate the effectiveness of FSST 2.0 (family supportive supervisor training plus support for use of family and sick leaves) using a randomized control trial design.

  • Phase of the Trial Based on the NIH's definition, the current study is a Phase III clinical trial, which usually involves several hundred or more human subjects, for the purpose of evaluating an experimental intervention in comparison with a standard or controlled intervention or comparing two or more existing treatments.
  • Type of trial - a randomized-control trial
  • Randomization strategy

    • Randomization method The current study employs a cluster randomization strategy to assign organizations to either Condition A (intervention group) or Condition B (control group) for a few key reasons. First, although only the supervisors will receive the training, the effectiveness of the training will be assessed at the employee' level, thereby needing a nested data structure. Second, cluster randomization is effective in reducing contamination (Puffer et al., 2005). Third, when the intervention is offered at a group level, cluster randomization increases the external validity of the results (Donner & Klar, 2000). Within each organization, we will use a balanced group randomization strategy such that there will be an equal number of workgroups/teams/departments in the intervention or control condition. In the event that there is an odd number of such units, a slight imbalance (i.e., groups per condition) will be off by one group, which has minimal impact on statistical power to detect intervention effects.
    • Unit of randomization - organization
    • Allocation ratio - the same number of teams (one supervisor and at least 6 employees) will be recruited in both organization
    • Timing of randomization - before the baseline assessment
    • The statistician of the study will generate and implement the randomization schema.
  • Specification of the number of study groups/arms - 2
  • Duration of the study intervention - 6 months
  • Follow-up period - 3 and 5 months after the intervention
  • Name and brief description of study intervention FSST 2.0 is a workplace intervention package designed to increase supervisors' family and leave supportive behaviors and leave supportive behaviors. The package includes Workplace Assessment tool, 2 30-45-minute online training modules (family-supportive supervisor training and supervisors' leave supportive behavior training), a webinar, behavior training, and organizational reports.
  • Control group The current trial employs a wait-list control group, "whereby participants will receive the usual care and will later receive the intervention in addition to the usual care" (Kinser & Robins, 2013, p.2).

One or more organization will be randomly assigned to receive the intervention and the other organization(s) will serve as a wait-list control group.

Mangers in the intervention group will be asked to:

  1. Complete a baseline online survey.
  2. Take the Family Supportive Supervisor Training online (FSST) - http://wlhmodule1.s3-website.us-east-2.amazonaws.com/
  3. Take the Supervisor Support for Leave Use module training online - http://wlhmodule2.s3-website.us-east-2.amazonaws.com/
  4. Track their behaviors for two weeks
  5. Participate in a webinar with the opportunity to ask Q & A and make comments.

7. Complete up to 2 post-training surveys. 8. Focus groups may also be conducted to get feedback on the training after the study is over.

Employees in the control group and employees in both groups will be asked to:

1. Complete a base line and follow up surveys over the course of 5 months.

The wait list control group will be offered the training after the trial is over.

Study Type

Interventional

Enrollment (Actual)

1175

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Indiana
      • West Lafayette, Indiana, United States, 47907
        • Purdue University

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • To be 18 years and older
  • To be a supervisor with at least six employees or an employee of a participating supervisor

Exclusion Criteria:

  • There is no exclusion criterion.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Group - Managers

Mangers in the intervention group will be asked to:

  1. Complete an online survey;
  2. Take the Family Supportive Supervisor Training online (FSST);
  3. Take the Supervisor Support for Leave Use module;
  4. Track their behaviors for two weeks;
  5. Participate in a webinar and have the opportunity to ask questions and give comments;
  6. Complete a post-training survey;
  7. 8-10 managers may also participate in the focus group.
FSST 2.0 is a workplace intervention package designed to increase supervisors' family and leave supportive behaviors and leave supportive behaviors. The package includes Workplace Assessment tool, 2 45-60 minute online training modules (family-supportive supervisor training and supervisors' leave supportive behavior training), a webinar, behavior training, and individualized feedback reports.
Other Names:
  • FSST 2.0
No Intervention: Control Group - Managers

Managers in the control group will be asked to:

1. Complete an online survey three times over the course of 5 months.

Experimental: Intervention Group - Employees

Employees in the intervention group will be asked to:

1. Complete an online survey three times over the course of 6 months.

FSST 2.0 is a workplace intervention package designed to increase supervisors' family and leave supportive behaviors and leave supportive behaviors. The package includes Workplace Assessment tool, 2 45-60 minute online training modules (family-supportive supervisor training and supervisors' leave supportive behavior training), a webinar, behavior training, and individualized feedback reports.
Other Names:
  • FSST 2.0
No Intervention: Control Group - Employees

Employees in the control group will be asked to:

1. Complete an online survey three times over the course of 5 months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Family Supportive Supervisor Behaviors
Time Frame: 5 months after the intervention

Family supportive supervisor behavior scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Leave Supportive Supervisor Behaviors
Time Frame: 5 months after the intervention

Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Work-family Conflict
Time Frame: 5 months after the intervention

Work family conflict scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (worse outcome). Negative scores = decrease in scores over time (better outcome).

5 months after the intervention
Change in Emotional Exhaustion
Time Frame: 5 months after the intervention

Emotional exhaustion scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (worse outcome). Negative scores = decrease in scores over time (better outcome).

5 months after the intervention
Change in Employee's Leave Use
Time Frame: 5 months after the intervention

Number of days of leave used for sick or family leave in the past 6 months. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time. Negative scores = decrease in scores over time.

Note: higher scores do not represent better or worse outcomes. They are descriptions of use needed for sick or family leave.

5 months after the intervention
Change in Turnover Intentions
Time Frame: 5 months after the intervention

Turnover intentions scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (worse outcome). Negative scores = decrease in scores over time (better outcome).

5 months after the intervention
Change in Control Over Work
Time Frame: 5 months after the intervention

Control over work scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Boundary Countrol
Time Frame: 5 months after the intervention

Boundary control scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Work-life Climate
Time Frame: 5 months after the intervention

Work-life climate scale. Original scale: Minimum value = 1, Maximum value = 5. Higher scores = expected to make more family sacrifices. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (worse outcome). Negative scores = decrease in scores over time (better outcome).

5 months after the intervention
Change in Work-to-family Positive Spillover
Time Frame: 5 months after the intervention

WTF positive spillover scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in General Supervisor Support
Time Frame: 5 months after the intervention

General supervisor support scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Supervisor Performance Support
Time Frame: 5 months after the intervention

Supervisor performance support scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Job Satisfaction
Time Frame: 5 months after the intervention

Job satisfaction scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Job Performance
Time Frame: 5 months after the intervention

Job performance scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Organizational Commitment
Time Frame: 5 months after the intervention

Organizational commitment item. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Perceived Health
Time Frame: 5 months after the intervention

Perceived health item. Original scale: Minimum value = 1, Maximum value = 5. Higher scores = better health. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (better outcome). Negative scores = decrease in scores over time (worse outcome).

5 months after the intervention
Change in Psychological Distress
Time Frame: 5 months after the intervention

Psychological distress scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (worse outcome). Negative scores = decrease in scores over time (better outcome).

5 months after the intervention
Change in Perceived Stress
Time Frame: 5 months after the intervention

Perceived stress scale. Original scale: Minimum value = 1, Maximum value = 5. Reported numbers represent change in these values over time: Time 3 (5-months post-baseline survey) - Time 1 (baseline survey) scores.

Positive scores = increase in scores over time (worse outcome). Negative scores = decrease in scores over time (better outcome).

5 months after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Ellen E Kossek, Ph.D., Work Life Help LLC

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 Major Dates

Study Start (Actual)

October 27, 2022

Primary Completion (Actual)

May 30, 2023

Study Completion (Actual)

May 30, 2023

Study Registration Dates

First Submitted

August 30, 2021

First Submitted That Met QC Criteria

October 4, 2021

First Posted (Actual)

October 15, 2021

Study Record Updates

Last Update Posted (Actual)

October 8, 2024

Last Update Submitted That Met QC Criteria

September 24, 2024

Last Verified

September 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All de-identified data and referenced resources from a publication will be made available by depositing them at dataverse.org. The dataset will include variables used for the publication with an accompanying codebook containing variables labels and codes in XLSX format. Metadata will be prepared as an XML file, which is compliant with the Data Documentation Initiative (DDI) specification.

The data and metadata from a publication will be made available by the online publication date.

The location of the public-use data and how to access the data, as well as acknowledgments of the repository and funding source, will be identified in any publications and presentations about these data.

IPD Sharing Time Frame

The data and metadata from a publication will be made available by the online publication date.

IPD Sharing Access Criteria

The data will be deposited and made available through dataverse.org for easy access to qualified researchers and analysts ( i.e., only those affiliated with a university or similar organization that is listed on the Dataverse website as qualified users). The data will be available for use only for research purposes such as replication and secondary studies. User registration will be required in order to access or download files from dataverse.org.

IPD Sharing Supporting Information Type

  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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