Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02652208 · ClinicalTrials.gov registry record · NA

Comparative Effectiveness of Decision Aids for Stable Chest Discomfort

A NA study, sponsored by Massachusetts General Hospital.

Completed
Registry status
NA
Development phase
34
Enrollment target

NCT02652208: Completed NA study, sponsored by Massachusetts General Hospital.

NCT02652208 is a NA study that has completed, run by Massachusetts General Hospital. The registered enrollment target is 34 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT02652208, a NA study, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
NA
Development phase
34 participants
Enrollment target

Study Summary

The purpose of the study is to compare two different types of decision support materials for patients considering treatment for chest pain or chest discomfort from heart disease.

Primary Outcome

Six multiple choice knowledge items covered important facts patients should know about chest pain or discomfort and treatments. A total knowledge score (0-6) was created by summing the total number of correct responses. A missing knowledge response was marked as incorrect. Any survey with more than three missing knowledge responses did not get a total knowledge score. A higher score indicates higher knowledge on the topic. Both decision aids provided information for answering all knowledge items

Interventions

  • BEHAVIORAL Video decision aid
  • BEHAVIORAL Online decision aid

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2016-01
Est. Completion 2016-11
Phase NA
Massachusetts General Hospital

2,032 total trials

What the finished NCT02652208 record still lists

NCT02652208 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Video decision aid is the first listed.

NCT02652208 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02652208 about?

NCT02652208 is a clinical study titled "Comparative Effectiveness of Decision Aids for Stable Chest Discomfort". The purpose of the study is to compare two different types of decision support materials for patients considering treatment for chest pain or chest discomfort from heart disease.

What is the current status of trial NCT02652208?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2016-01. Estimated completion is 2016-11.

What interventions are being tested in trial NCT02652208?

The interventions under investigation include: Video decision aid (BEHAVIORAL), Online decision aid (BEHAVIORAL).

Who is sponsoring clinical trial NCT02652208?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02652208's enrollment target sits among peer trials

34 1570th of 2000 higher than 427 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02897063 · 34 participants · Phase 1

    Effects of Midodrine and Droxidopa on Splanchnic Capacitance in Autonomic Failure

  • NCT03906617 · 34 participants · Phase 4

    Bupivacaine/Epinephrine +Dexamethasone vs. Liposomal Bupivacaine

  • NCT03992378 · 34 participants · NA

    Neuromodulation to Regulate Inflammation and Autonomic Imbalance in Sepsis

  • NCT04047849 · 34 participants · Phase 4

    Latency Antibiotics in Previable PPROM, 18 0/7- 22 6/7 WGA

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02652208, the US trial registry maintained by the National Library of Medicine. NCT02652208 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.