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An intervention to improve cooperation between absent employees and their employers.

Improved cooperation between absent employees and their employers.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22455
Enrollment
140
Registered
2011-11-08
Start date
2011-03-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

All health conditions, except for terminal illnesses

Interventions

Intervention group: 1. Absent employees and their employers use a guideline to structure and intensify their cooperation. Among others, this guideline advises employees and employers about their meet
2. Every four to six weeks, employees and employers fill out a questionnaire about their cooperation
3. In case the results of the questionnaire point out a lack of cooperation, employees and employers are supported by a third actor (an occupational physician or other professional) to cooperate with

Sponsors

Sponsor: Stichting Instituut GAK Performer: Maastricht University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The inclusion criteria for the employees are that they: 1. Are on sick leave for at least two weeks; 2. Expect to be absent from work for at least four working weeks; 3. Are appointed to work for at least twelve hours per week; 4. Are aged between 18 and 60 years old. Employees can participate in the study only when their employers are willing to participate as well.

Exclusion criteria

Exclusion criteria: The exclusion criteria for the employees are that they: 1. Expect to resume work within four weeks after they called in sick; 2. Have a labour contract that ends within eighteen months; 3. Suffer from a terminal illness; 4. Are absent for more than eighth weeks. According to Dutch law, a return to work plan is composed before eighth weeks of absence. If such as plan exists, the intervention may interfere with the plan; 5. Take part in another study or receive other kinds of support (such as coaching) to return to work.

Design outcomes

Primary

MeasureTime frame
Proximal outcomes: 1. Outcome name: Mutual trust measured by means of among others a self-developed questionnaire. Time points: Every four to six weeks until the employee returns to work; 2. Outcome name: Mutual dependency with a self-developed questionnaire. Time points: Every four to six weeks until the employee returns to work; 3. Outcome name: Cooperation with among others self-developed questionnaires. Time points: Every four to six weeks until the employee returns to work. Distal outcomes: 1. Outcome name: Participation (sickness absence) with the Prodisq. Time points: 0, 6 and 12 months; 2. Outcome name: Health with parts of the SF-36. Time points: 0, 6 and 12 months; 3. Outcome name: Quality of life with the EQ-5D-5L. Time points: 0, 6 and 12 months; 4. Outcome name: Care consumption with the TIQP. Time points: 0, 6 and 12 months.

Secondary

MeasureTime frame
Outcome name: Satisfaction about support provided by the third actor (measured by means of a self-developed questionnaire in intervention group only). Time points: As soon as possible after the employee returned to work.

Contacts

Public ContactNicole Hoefsmit

Maastricht University, Researchschool Caphri Department of Social Medicine P.O. Box 616

n.hoefsmit@maastrichtuniversity.nl+31 (0)43 3881709

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)