Documenting and Understanding the Invisible Load

Last registered on February 26, 2026

Pre-Trial

Trial Information

General Information

Title
Documenting and Understanding the Invisible Load
RCT ID
AEARCTR-0016624
Initial registration date
August 26, 2025

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
September 01, 2025, 3:19 PM EDT

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

Last updated
February 26, 2026, 11:58 AM EST

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

Locations

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Primary Investigator

Affiliation
Tufts University

Other Primary Investigator(s)

PI Affiliation
Brigham Young University
PI Affiliation
Syracuse University

Additional Trial Information

Status
On going
Start date
2025-08-26
End date
2027-12-31
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
We study how childcare and eldercare decision-makers respond to email inquiries from parents or children. In a US field experiment with daycare and eldercare centers, we send an email that varies (i) whether the message frames the situation as an exogenous emergency (“our caregiver is moving unexpectedly”), as an endogenous oversight (“we dropped the ball”), or does not specify a reason reason (ii) whether the sender is male or female (by using a male or female sounding name) and (iii) whether the sender is a single parent in the case of childcare. We measure if and how centers respond (reply rate and speed), whether they offer an appointment or a spot (and timing), and the tone/helpfulness of replies.
External Link(s)

Registration Citation

Citation
Buzard, Kristy, Laura Gee and Olga Stoddard. 2026. "Documenting and Understanding the Invisible Load." AEA RCT Registry. February 26. https://doi.org/10.1257/rct.16624-1.1
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Experimental Details

Interventions

Intervention(s)
In the interest of preserving the integrity of the experiment, the intervention is being described in full in the experimental design sections that will remain hidden until the experiment is completed.
Intervention Start Date
2025-09-01
Intervention End Date
2027-12-31

Primary Outcomes

Primary Outcomes (end points)
Reply received (0/1).
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
· ReplyLatency: Continuous measure of time to reply (in hours or days) from when the email was sent. This is the primary definition for latency and will be used in all main analyses.
· Tone / sentiment of response.
· Length of reply (word/character count).
. Content: Measures based on the content of the response (e.g. offer to schedule a tour/appointment, provision of alternative options or helpful resources, etc.)
Note on robustness: While the primary definition of ReplyLatency is continuous, for robustness and interpretability we may also categorize response time into bins (e.g., within 1 day, within 7 days).

Secondary Outcomes (explanation)

Experimental Design

Experimental Design
In the interest of preserving the integrity of the experiment, the experimental design is being described in full in the experimental design sections that will remain hidden until the experiment is completed.
Experimental Design Details
Not available
Randomization Method
Randomization done by computer. Stratification ensures balance across demographic attributes of the centers like provider type, region, and other characteristics.
Randomization Unit
Daycare or eldercare center.
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
We included about 2000 daycares in the first pilot study. And we plan to include approximately 3000 daycare centers and 1500 eldercare centers in the second pilot study. Each center represents one cluster, as responses are measured at the center level. Following the pilot, we will update our power calculations based on the observed effect sizes.
Sample size: planned number of observations
Because each center is contacted only once, the total number of observations will also be 2000 & 4500 carecenters for the primary outcomes in the first and second pilots. Each observation corresponds to one unique center’s response (or non-response) to our email. The secondary outcomes (e.g. sentiment of the email response) will be determined by the response rate to our various treatments.
Sample size (or number of clusters) by treatment arms
We are running a 3×6 factorial design with eighteen treatment arms with equal size samples in each treatment:
T1_M_S: “Unexpected Need” message, male sender, single parent
T1_F_S: “Unexpected Need” message, female sender, single parent
T2_M_S: “Dropped the ball” message, male sender, single parent
T2_F_S: “Dropped the ball” message, female sender, single parent
T3_M_S: No reason message, male sender, single parent
T3_F_S: No reason message, female sender, single parent
T1_M_N: “Unexpected Need” message, male sender, non-single
T1_F_N: “Unexpected Need” message, female sender, non-single
T2_M_N: “Dropped the ball” message, male sender, non-single
T2_F_N: “Dropped the ball” message, female sender, non-single
T3_M_N: No reason message, male sender, non-single
T3_F_N: No reason message, female sender, non-single
T1_M_C: “Unexpected Need” message, male sender, child
T1_F_C: “Unexpected Need” message, female sender, child
T2_M_C: “Dropped the ball” message, male sender, child
T2_F_C: “Dropped the ball” message, female sender, child
T3_M_C: No reason message, male sender, child
T3_F_C: No reason message, female sender, child
We plan to have 2000 centers and 4500 centers in the first and second pilots.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
See pre-analysis plan for power calculation details
IRB

Institutional Review Boards (IRBs)

IRB Name
Tufts SBER IRB
IRB Approval Date
2021-04-21
IRB Approval Number
STUDY00001527
IRB Name
Tufts SBER IRB
IRB Approval Date
2026-02-19
IRB Approval Number
STUDY00006726
Analysis Plan

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