Does monitoring adversely affect worker performance? Evidence from a natural field experiment

Last registered on July 18, 2022

Pre-Trial

Trial Information

General Information

Title
Does monitoring adversely affect worker performance? Evidence from a natural field experiment
RCT ID
AEARCTR-0003475
Initial registration date
October 22, 2018

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
October 23, 2018, 9:28 PM EDT

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Last updated
July 18, 2022, 2:56 AM EDT

Last updated is the most recent time when changes to the trial's registration were published.

Locations

Region
Region

Primary Investigator

Affiliation
University of Fribourg

Other Primary Investigator(s)

PI Affiliation
University of Fribourg

Additional Trial Information

Status
On going
Start date
2018-07-04
End date
2023-12-31
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
We conduct a natural field experiment with remote workers to assess potential adverse effects of monitoring.
External Link(s)

Registration Citation

Citation
Herz, Holger and Christian Zihlmann. 2022. "Does monitoring adversely affect worker performance? Evidence from a natural field experiment." AEA RCT Registry. July 18. https://doi.org/10.1257/rct.3475-7.799999999999998
Former Citation
Herz, Holger and Christian Zihlmann. 2022. "Does monitoring adversely affect worker performance? Evidence from a natural field experiment." AEA RCT Registry. July 18. https://www.socialscienceregistry.org/trials/3475/history/149858
Experimental Details

Interventions

Intervention(s)
A control device is implemented in a natural work environment. We will investigate how workers react to such an implementation of control: Is there a negative behavioural reaction, i.e. do workers lower their effort once control is implemented?

Two groups:
1. Control group - incomplete contract (no control device)
2. Treatment group - contract with a minimum performance requirement (a imperfect control device)
Intervention Start Date
2018-12-10
Intervention End Date
2020-03-12

Primary Outcomes

Primary Outcomes (end points)
Primary outcome is how workers performance is affected by the random assignment to the control and treatment group. Hence, key outcome variable is workers performance. For further details, please refer to the pre-analysis plan.
Primary Outcomes (explanation)
For further details, please refer to the pre-analysis plan.

Secondary Outcomes

Secondary Outcomes (end points)
For further details, please refer to the pre-analysis plan.
Secondary Outcomes (explanation)
Please refer to the pre-analysis plan.

Experimental Design

Experimental Design
The (public) description of the experimental design is kept to its minimum to avoid experimenter demand effects. The (hidden) description will become public once the study is completed and will help you to understand the design in further detail.

In short, in a real labor market, we create two groups: One group receives an incomplete contract and is not subject no any controlling or monitoring device. The other group receives a more complete contract with a minimum performance requirement as a control device. First, all workers are assigned to an incomplete contract (HIT1). In a second stage, workers are assigned to one of the two mentioned groups (HIT2) and perform again a real-effort task.
Experimental Design Details
For further details, please refer to the pre-analysis plan.
Randomization Method
Randomization done by a computer software (Otree).
Randomization Unit
Individual
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
no clustered treatment.
Sample size: planned number of observations
For the calculation of power and the planned number of observations, please refer to the pre-analysis plan.
Sample size (or number of clusters) by treatment arms
For the calculation of power and the planned number of observations, please refer to the pre-analysis plan.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
For the calculation of power and the planned number of observations, please refer to the pre-analysis plan.
Supporting Documents and Materials

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IRB

Institutional Review Boards (IRBs)

IRB Name
Internal Review Board of the Department of Psychology, University of Fribourg
IRB Approval Date
2018-07-02
IRB Approval Number
2018-393
Analysis Plan

Analysis Plan Documents

Memo concerning pre-analysis plan 22 Oct 2018 (dated 10 Dec 18)

MD5: 3c2fb1349c446287dcf94d53c636a42f

SHA1: 71f86dd9ed7960194f8a2dd71237db18f8ee939b

Uploaded At: December 10, 2018

Pre-analysis Plan 8 March 2020 - REPLICATION

MD5: 0ed3485ff554301cc506edaa91167cd6

SHA1: a629d2dbbbee05bb833430403ae95cd916f25611

Uploaded At: March 08, 2020

Pre-analysis Plan 22 Oct 2018

MD5: 419fe1daec88d8ece8679a6a8957f2f6

SHA1: d51d043e57bcead7f7cbb3e264f85878dc4af0ad

Uploaded At: October 23, 2018

Post-Trial

Post Trial Information

Study Withdrawal

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Intervention

Is the intervention completed?
No
Data Collection Complete
Data Publication

Data Publication

Is public data available?
No

Program Files

Program Files
Reports, Papers & Other Materials

Relevant Paper(s)

Reports & Other Materials