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Preferences for Religious Giving - follow-up

Last registered on May 07, 2019

Pre-Trial

Trial Information

General Information

Title
Preferences for Religious Giving - follow-up
RCT ID
AEARCTR-0003989
Initial registration date
May 06, 2019

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 07, 2019, 10:22 AM EDT

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

Locations

Primary Investigator

Affiliation
OECD

Other Primary Investigator(s)

PI Affiliation
TSE, IAST
PI Affiliation
TSE
PI Affiliation
World Bank
PI Affiliation
TSE, IAST

Additional Trial Information

Status
In development
Start date
2019-05-06
End date
2019-06-01
Secondary IDs
Abstract
This study investigates why people give money to religious organizations, using a laboratory experiment in Accra, Ghana. In particular, we seek to understand to what extent churches provide informal insurance to households. Although contracts exist with quite low premiums, less than 1% of Ghanaian households are insured. With 96% of inhabitants reporting themselves to be religious, beliefs in a God play a major role in the daily lives of many Ghanaians. Much of this religious activity is backed by regular and significant contributions to the church through tithes, regular offering, and other forms of giving. We offer households a range of incentivized choices between donations to religious organizations and other financial options. We implement treatments including increasing the perceived risk of life accidents and the provision of free insurance to observe the effect on the demand for religious giving. We also compare how these treatments effects vary for individuals participating in the experiment during "revival weeks" - weeks of intense church participation, with others participating during normal weeks. This study is a follow-up for study AEARCTR-0000558.
External Link(s)

Registration Citation

Citation
Auriol, Emmanuelle et al. 2019. "Preferences for Religious Giving - follow-up." AEA RCT Registry. May 07. https://doi.org/10.1257/rct.3989-1.0
Former Citation
Auriol, Emmanuelle et al. 2019. "Preferences for Religious Giving - follow-up." AEA RCT Registry. May 07. https://www.socialscienceregistry.org/trials/3989/history/46107
Sponsors & Partners

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Experimental Details

Interventions

Intervention(s)
The study will be conducted in two parts: first, a survey covering demographic
questions and religious beliefs and behaviour and second, a decision task
presenting participants with binary choices on ways to spend 11GHS.
Our interest is 1) to investigate the effects of increasing the salience of life accidents risk (informaton treatment) and the effect of providing individuals an insurance policy (insurance treatment) on their preferences for making donations to different causes, and 2) how these effects differ when individuals participate in the experiment during normal weeks and when participation happens during "revival weeks" - weeks of intense church participation and in which churchgoers donate much more than in an average week.
Intervention Start Date
2019-05-06
Intervention End Date
2019-06-01

Primary Outcomes

Primary Outcomes (end points)
The key outcome variable is the difference in donations between individuals endowed with the information treatment and individuals with the insurance treatment.
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
The secondary outcome is the difference between treatments effects for individuals that participate in the experiment during revival and those that participate during normal weeks.
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
We divide the subjects into three groups; 1/3 of the subjects will be allocated with a life insurance policy, 1/3 of the
participants will be told about, but not endowed with, this insurance policy, and 1/3 of the participants will form the control group.
The study participants will be recruited from the Assemblies of God church and half of them will be randomly invited to participation in the study during a revival week while the other half will be invited to participate in a normal week.
Experimental Design Details
Church participants will be recruited from the Assemblies of God church population. They will be approached in advance and invited to show up to a specific session. Participants will be met at their own church premises and driven to the experiment location. Anyone above the age of 18, and the mental and physical capacity to answer questions for 1.5 hours will be eligible to participate in the experiment. The experiment room will be equipped with 10 tablets. All locations will also have a black/whiteboard. The choices to be played and their associated tags (A, B , C,…J) will be prominently displayed for the duration of the experiment. Participants will have to choose how to allocate 11GHS between 2 options. The alternatives are: keeping the money, donating to the thanksgiving offering of the National Prayer Week, donating to the Street Children Empowerment Fund, making a private donation directly to their church and making a non-anonymous donation directly to their church. All these choices are kept anonymous, except for the public choice to give to the church, for which the name of the participant and the amount he chose to give is communicated to the Pastor.
Randomization Method
Randomization between information and insurance treatments is performed at the session level and done by the draw a sealed enveloppe by a participant.
Randomization between particpation in a normal or revival week is performed at the participant level and done by random draw from a box without replacement.
Randomization Unit
Randomization between information and insurance treatments is performed at the session level.
Randomization between particpation in a normal or revival week is performed at the participant level.
Was the treatment clustered?
Yes

Experiment Characteristics

Sample size: planned number of clusters
At least 64 sessions of 10 participants
Sample size: planned number of observations
640 participants
Sample size (or number of clusters) by treatment arms
Approx. 100 individuals per treatment (6 treatments)
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
This round of experiments is under-powered. The primary aim is to pool the data from this follow-up with data from previous rounds for non-revival weeks and validate the main effects for non-revival weeks. The secondary objective is to provide preliminary evidence for how treatment effects differ between revival and non-revival weeks.
IRB

Institutional Review Boards (IRBs)

IRB Name
IRB Approval Date
IRB Approval Number

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