Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06678347

Leadership for Recovery: Effects of an Intervention Programme for First-line Healthcare Managers on Employees' Recovery

Led by Karolinska Institutet · Updated on 2024-11-18

960

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate a group-based intervention programme called "Leadership for Recovery" designed for first-line healthcare managers in Swedish hospital settings. The study focuses on whether strengthening managers' own recovery strategies and their leadership focused on promoting employee recovery can improve the recovery, including sleep, health, cognition, work-life balance, and job retention among healthcare employees. The trial is a cluster randomized controlled study comparing employees whose managers participate in the programme to those whose managers do not. The intervention consists of 6 group sessions spread over approximately 6 months, combining educational and reflective activities to support managers' recovery and enhance their ability to promote recovery among their employees. Managers are randomly assigned to either the intervention group, which receives the programme, or a control group that does not participate during the study period but may join after follow-up. Employees of both groups are invited to participate and their recovery and health outcomes will be compared. Participants will complete surveys before the intervention begins, shortly after the managers complete five sessions, and again one year after baseline. A voluntary subset will also keep diaries and wear actigraphy wristbands to objectively measure sleep for 7-day periods at baseline and follow-up. Researchers will assess primary outcomes related to recovery and sleep, and secondary outcomes such as general health, burnout, cognition, work performance, and work-life interference. Data analysis will follow intention-to-treat principles and include safety monitoring through ongoing questionnaires.

CONDITIONS

Brief Title

Leadership for Recovery: Evaluation of an Intervention Programme for First-line Healthcare Managers

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Managers must be first-line managers of nursing or laboratory staff in hospital care
  • Employees must have a first-line manager who participates in the study
  • Managers must have at least 6 months of work experience as a manager at baseline
  • Managers must be employed at least 50% as a manager
  • Participants must be aged 18 years or older
Not Eligible

You will not qualify if you...

  • Managers with less than 6 months' work experience as a manager at baseline
  • Managers employed less than 50% as a manager
  • Employees who are casual workers
  • Employees with less than 6 months' work experience in their profession at baseline (for diary and actigraphy study only)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Outpatient Treatment

Duration - Approximately 6 months

Managers participate in a group-based intervention programme focusing on promoting their own recovery and leadership to enhance employee recovery. The programme consists of 6 group sessions delivered over approximately 6 months.

6 group sessions (in-person)

Monitoring

Duration - 1 year

Employees complete surveys at baseline, post-intervention, and follow-up to measure recovery, health, cognition, work performance, and other outcomes. A subsample also participates in diary and actigraphy sleep monitoring at baseline and follow-up.

3 survey assessments and 2 periods of 7-day diary and actigraphy monitoring

Trial Site Locations

Total: 2 locations

1

Sahlgrenska Universitetssjukhuset

Gothenburg, Sweden

Actively Recruiting

2

Karolinska Universitetssjukhuset

Stockholm, Sweden

Actively Recruiting

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Research Team

A

Anna Dahlgren, Docent

M

Majken Epstein, PhD Student

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Published Research Related To This Trial

Randomised control trial of a proactive intervention supporting recovery in relation to stress and irregular work hours: effects on sleep, burn-out, fatigue and somatic symptoms.

Anna Dahlgren, Philip Tucker, Majken Epstein...

https://pubmed.ncbi.nlm.nih.gov/35074887