Experimental Design
Design:
Parallel-arm, between-subjects randomized controlled trial conducted online. Participants are randomly assigned (1:1:1) to one of three arms at the start of the survey:
(A) a brief prosocial message framed in religious language;
(B) a closely matched prosocial message framed in scientific/psychology language; or
(C) no message (control).
Messages are similar in length and readability; only the framing differs. No deception is used.
Eligibility & setting:
Adults (18+) completing a single session on a standard online survey platform. Participation is anonymous and voluntary; respondents may skip questions.
Timing & flow:
After providing consent, participants are randomly assigned to one of the three conditions. The assigned message (or no message) is displayed on its own screen. Immediately afterward, participants complete the outcome measures within the same session.
Primary outcomes (confirmatory):
Self-reported religiosity measured immediately after the intervention using two outcomes:
Importance of God in life (0–10 scale; 0 = not at all important, 10 = very important);
Desire to pray often, constructed as a binary indicator equal to one if respondents report praying at least once per day.
Secondary outcomes (public summary):
A broader set of attitudinal and behavioral measures, including:
religious beliefs (e.g., belief in God, afterlife);
religious attitudes (e.g., views on religion vs. science);
religious behavior (e.g., church attendance);
moral and social attitudes (e.g., abortion, homosexuality, immigration, same-sex marriage);
behavioral preferences (e.g., revenge, punishment, forgiveness);
political ideology and vaccination status;
additional preference measures (e.g., self-comparison, willingness to sacrifice for the future).
Randomization & masking:
Treatment assignment is implemented automatically by the survey platform’s randomizer. Participants are not informed about the existence or content of alternative messages.
Analysis (high-level):
We estimate intent-to-treat effects by comparing average outcomes across groups using two-sided tests at α = 0.05. The primary confirmatory contrast is the scientific framing relative to the control group. Secondary contrasts include religious vs. control and scientific vs. religious framing. Secondary outcomes are analyzed as exploratory with appropriate consideration of multiple testing.
Exposure & quality controls (summary):
A minimum on-screen exposure time is imposed for the message. A simple attention check is included to encourage data quality. Any exclusion criteria are prespecified elsewhere in the preregistration.