| Protocol ID | NCT04859114 |
| Registration Date | 2021-04-26 |
| Status | completed |
| Sponsor | Medical College of Wisconsin |
| Country | United States |
| Industry | not industry |
| Blinding | blinded |
| Center Type | singel-center RCT |
| Scope | national RCT |
| First Patient In | 2021-06-07 |
| Last Patient Out | 2021-06-22 |
| Publication | y |
| Gender % | FEMALE |
| Mean Age | 18 Years - 45 Years |
NCT04859114
Effect of Presenting Survival Information as Text or Pictograph During Periviable Birth
| Field |
OPENAI
gpt-4o 3438ms / 9291 tok |
CLAUDE
claude-sonnet-4-20250514 4823ms / 10693 tok |
GLM
glm-5.1 6674ms / 9438 tok |
Review |
|---|---|---|---|---|
| rct_type |
parallel RCT
N/A → parallel RCT
shaky reasoning✓ Unanimous
Initial: N/A
Requery: parallel RCT — Participants are randomized to different arms receiving distinct intervention formats without mention of crossover or cluster design.
|
parallel RCT
parallel RCT → parallel RCT
shaky reasoning✓ Unanimous
Initial: parallel RCT
Requery: parallel RCT — This is a 2x3 factorial design where participants are randomly assigned to one of six arms (combinations of data presentation format and survival percentage) and each participant receives only one intervention, making it a parallel randomized controlled trial.
|
parallel RCT
parallel RCT
shaky reasoning✓ Unanimous
Initial: parallel RCT
|
OK |
| cancer_status | non-cancer | non-cancer | non-cancer | OK |
| non_cancer_spec | N/A | N/A | N/A | OK |
| setting_patient | outpatient | outpatient | outpatient | OK |
| setting_place | other | other | other | OK |
| feasibility | fully powered RCT | fully powered RCT | fully powered RCT | OK |
| intervention_pharmacologic | no | no | no | OK |
| intervention_chemo_immuno_radio | no | no | no | OK |
| intervention_complementary | no | no | no | OK |
| intervention_device | no | no | no | OK |
| intervention_psychological | no | no | no | OK |
| intervention_complex | no | no | no | OK |
| intervention_acp | no | no | no | OK |
| intervention_music | no | no | no | OK |
| intervention_screening | no | no | no | OK |
| intervention_palliative | no | no | no | OK |
| intervention_education |
no
no → no
shaky reasoning✓ Unanimous
Initial: no
Requery: no — The primary focus of the trial is on how different formats of outcome data presentation affect decision-making, not on educating participants about the decision-making process itself.
|
no
yes → no
shaky reasoning✓ Unanimous
Initial: yes
Requery: no — This study tests different formats of presenting survival information (text vs pictographs) to examine decision-making preferences, rather than providing educational training or programs to participants.
|
no
no → no
shaky reasoning✓ Unanimous
Initial: no
Requery: no — The trial evaluates the effect of different formats of data presentation (text vs. pictograph) on decision making, rather than primarily providing an educational or training program.
|
OK |
| intervention_digital | no | no | no | OK |
| intervention_other |
no
yes → no
shaky reasoning✓ Unanimous
Initial: yes
Requery: no — The trial involves a behavioral intervention related to data presentation formats, which fits neither the residual category nor the exceptions listed.
|
no
no → no
shaky reasoning✓ Unanimous
Initial: no
Requery: no — This is a psychological intervention testing different formats of presenting medical information to influence decision-making behavior, which fits the psychological intervention category.
|
no
yes → no
shaky reasoning✓ Unanimous
Initial: yes
Requery: no — The trial involves comparing how different formats of presenting information (text vs. pictograph) affect decision-making, which falls under psychological or educational interventions.
|
OK |
| outcome_symptom | no | no | no | OK |
| outcome_qol | no | no | no | OK |
| outcome_dignity | no | no | no | OK |
| outcome_cost | no | no | no | OK |
| outcome_other | yes | yes | yes | OK |
| pharmacologic_sub | N/A | N/A | N/A | OK |