Promoting regular labor supply among the urban poor

Last registered on September 09, 2022

Pre-Trial

Trial Information

General Information

Title
Promoting regular labor supply among the urban poor
RCT ID
AEARCTR-0009402
Initial registration date
May 08, 2022

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
May 09, 2022, 8:25 PM EDT

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

Last updated
September 09, 2022, 5:50 AM EDT

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

Locations

Region

Primary Investigator

Affiliation
UC Berkeley

Other Primary Investigator(s)

PI Affiliation
UC Berkeley
PI Affiliation
University of Pennsylvania
PI Affiliation
National University of Singapore

Additional Trial Information

Status
On going
Start date
2022-03-21
End date
2023-12-31
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
Low and irregular labor force participation, high labor turnover and absenteeism are major impediments to productivity in poor countries. We hypothesize that workers have difficulty providing regular labor supply in the formal sector because they might not a preference for doing so. We design an RCT with urban casual laborers in India, where laborers are provided incentives to boost their labor supply to urban labor stands -- their primary source of regular employment. We examine the persistence of effects on labor supply once incentives are removed.
External Link(s)

Registration Citation

Citation
Cefala, Luisa et al. 2022. "Promoting regular labor supply among the urban poor." AEA RCT Registry. September 09. https://doi.org/10.1257/rct.9402-1.1
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Experimental Details

Interventions

Intervention(s)
In this study, we hypothesize that workers’ preference for, and ability to maintain, long-term employment is malleable. We test this hypothesis by exploiting a habit-formation design, whereby we provide small financial incentives to attend daily to a randomly selected group of informal laborers for a limited period of time (6-8 weeks) and then observe labor market outcomes. The primary hypothesis we will test is that treated participants will attend the stand more often than Control participants not only in Phase 1 (incentives), but also in Phase 2 (follow-up phase, without incentives).
Intervention Start Date
2022-05-09
Intervention End Date
2022-10-31

Primary Outcomes

Primary Outcomes (end points)
Our primary outcome is attendance at the labor stand during phase 2.
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
We will measure impacts on employment levels and earnings.
Secondary Outcomes (explanation)
These two outcomes are considered secondary because: 1) they are self-reported leading to additional noise in the data, and 2) they are dependent on labor demand as well, which may vary across contexts. We will also collect supplementary data including: reasons for absences and a brief questionnaire on time use, habits, and identity.

Additional outcomes subject to feasibility. We are piloting to determine whether participants can be asked to wear pedometers for a portion of the study, in the hopes of providing an “objective” measure of the amount of work done. However, we will only analyze this data if we are able to incentivize participants to wear the devices regularly.

Similarly, we are attempting to partner with a construction firm to offer participants the choice of a “regular” job that is salaried and requires consistent attendance. Incentive compatible preferences for this type of work will be elicited and, if possible, a (small) random subset will be offered their choice at the end of the study. Take-up of the offer will be dependent on our being able to secure such a partner firm.
Additional outcomes subject to feasibility. We are piloting to determine whether participants can be asked to wear pedometers for a portion of the study, in the hopes of providing an “objective” measure of the amount of work done. However, we will only analyze this data if we are able to incentivize participants to wear the devices regularly.

Similarly, we are attempting to partner with a construction firm to offer participants the choice of a “regular” job that is salaried and requires consistent attendance. Incentive compatible preferences for this type of work will be elicited and, if possible, a (small) random subset will be offered their choice at the end of the study. Take-up of the offer will be dependent on our being able to secure such a partner firm.

Experimental Design

Experimental Design
The RCT will incentivize a subset of workers to increase their attendance at the stand, and then remove the incentives to examine the persistence of labor supply changes among treated participants.
Experimental Design Details
The RCT consists of three phases:
Baseline (3 weeks): which includes screening, baseline daily data collection on attendance and labor outcomes, randomization, and announcement of treatment conditions. Participants also take a survey—prior to learning their treatment status—on demographics and baseline beliefs about job search. Participants are tracked for 11 days to gather baseline data on labor supply habits.

Phase 1 (6-8 weeks): participants enter Phase 1 and are assigned to a Treatment group (which receives incentives to increase their labor supply) or a Control group (which receives matched but unconditional payments to address income effects). Payments, described in more detail below, are made at the end of each week. This phase may be extended slightly for groups with disruptions to Phase 1 (e.g. holidays, weather shocks, election periods).

Phase 2 (6–8 weeks): During Phase 2, incentive payments will be removed for both Treatment and Control groups, but participants will continue to be surveyed about their labor market outcomes.

Treatment conditions
1) Treatment (financial incentives) participants receive a fixed incentive payment for each day they attend the labor stand and arrive before a predetermined cutoff time (computed during baseline based on worker flows at the labor stand) from Monday to Saturday during Phase 1. In order to be eligible for an incentive payment, treatment participants need to be observed at the stand by a surveyor before the predetermined cutoff time. For festival days – when the field staff is not working – no payments are provided to either treatment or control participants. These days are communicated to participants in advance.

2) Control participants receive a weekly lump sum payment, unconditional on attendance, during Phase 1. The payment amount is determined by randomly matching each control individual with a treatment individual within the same stand-stratum. This process ensures that both the mean and variance of payments is similar across arms to avoid differential income effects, but prevents collusion. This random match between a control and treatment participant is carried out each week. During informed consent, control participants are told that the payment amount is chosen randomly by the computer.

In Phase 2 (after the removal of incentives), the treatment participants will no longer receive payments conditional on attendance at the stand. They will receive payments for survey completion which are the same between treatment and control groups throughout the study.

Randomization Method
The randomization is performed using Stata
Randomization Unit
Participants are randomly assigned at the individual level, stratified on stand, baseline attendance and baseline average daily wage earnings, to either the control arm or the treatment arm. Cut offs to determine the strata are computed using the median number of days of baseline attendance and the median baseline average self-reported daily wage from pilot stands.
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
We will enroll approximately 250-350 workers (depending on take-up at the stands) across approximately 15 stands in Chennai.
Sample size: planned number of observations
We will enroll approximately 350-500 workers (depending on take-up at the stands) across approximately 15 stands in Chennai.
Sample size (or number of clusters) by treatment arms
We plan to have half of the sample enrolled in the treatment arm and half in the control arm. Some variation may occur because of the difference size of the strata.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
IRB

Institutional Review Boards (IRBs)

IRB Name
Institute for Financial Management and Research
IRB Approval Date
2019-07-30
IRB Approval Number
IRB00007107
IRB Name
UC Berkeley
IRB Approval Date
2019-08-19
IRB Approval Number
#00006252
Analysis Plan

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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