FSST: Family Supportive Supervisor Training and Workplace Assessment Tool

Sponsor
Work Life Help (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05080426
Collaborator
National Institute on Aging (NIA) (NIH)
1,400
2
9

Study Details

Study Description

Brief Summary

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 of 200 managers and 1200 employees across 100 teams. Managers in the intervention group will complete pre- and post-intervention Workplace Assessments, 2 online training modules, 1 webinar. A small portion of the managers (8-10) will participate in the focus group. Managers in the control group and employees in both groups will complete pre- and post-intervention Workplace Assessments. The post-intervention Workplace Assessment will be completed 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 follow up survey after the 6 month trial.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Family Supportive Supervisor Training 2.0
N/A

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 their employees' levels, 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 team 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 - 9 months

  • Follow-up period - 6 and 9 months after the intervention

  • A single site trial - the Purdue University team will implement 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 individualized feedback 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). 3. Take the Supervisor Support for Leave Use module training online. 4. Track their behaviors for two weeks 5. Participate in a webinar 7. Complete up to 2 post-training surveys. 8. 8-10 managers will participate in the focus group.
Employees in the control group and employees in both groups will be asked to:
  1. Complete an online survey twice over the course of 6 months.

The wait list control group will be offered the training after the 6 months trial is over with a follow up survey.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The current study employs a cluster randomization strategy to assign organizations to either Condition A (intervention group) or Condition B (control group). One organization will be randomly assigned to the intervention and the other organization to the control group.The current study employs a cluster randomization strategy to assign organizations to either Condition A (intervention group) or Condition B (control group). One organization will be randomly assigned to the intervention and the other organization to the control group.
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
Family Supportive Supervisor Training and Workplace Assessment Tool
Anticipated Study Start Date :
Apr 1, 2022
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

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 7. Complete a post-training survey. 8. 8-10 managers will participate in the focus group. Employees in the intervention group will be asked to: 1. Complete an online survey twice over the course of 6 months.

Behavioral: Family Supportive Supervisor Training 2.0
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 and employees in the control group will be asked to: 1. Complete an online survey twice over the course of 6 months.

    Outcome Measures

    Primary Outcome Measures

    1. change in Family supportive supervisor behaviors [at baseline and 6 months after the intervention]

      Family supportive behavior scale Hammer et al., 2013

    2. change in Leave supportive supervisor behaviors [at baseline and 6 months after the intervention]

      To be developed

    Secondary Outcome Measures

    1. change in work-family conflict [at baseline and 6 months after the intervention]

      Matthews et al., 2010 work family conflict scale

    2. change in emotional exhaustion [at baseline and 6 months after the intervention]

      Barnett et al., 1999 emotional exhaustion scale

    3. change in depressive symptoms [at baseline and 6 months after the intervention]

      CES-D: Radloff, 1977

    4. change in employee's leave use [at baseline and 6 months after the intervention]

      number of days of leave used

    5. change in turnover intentions [at baseline and 6 months after the intervention]

      Boroff & Lewin, 1997 turnover intentions scale

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Work Life Help
    • National Institute on Aging (NIA)

    Investigators

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

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ellen Kossek, Basil S. Turner Distinguished Professor of Management, Work Life Help
    ClinicalTrials.gov Identifier:
    NCT05080426
    Other Study ID Numbers:
    • 2R42AG050347-02A1
    • 2R42AG050347-02A1
    First Posted:
    Oct 15, 2021
    Last Update Posted:
    Oct 15, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ellen Kossek, Basil S. Turner Distinguished Professor of Management, Work Life Help
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 15, 2021