CTMSS Pregnancy Registry

The CTMSS Research Committee leads efforts to promote and gather relevant clinical TMS data. The committee is currently seeking clinical safety and outcome data from CTMSS members who have treated pregnant patients with TMS.

Although a comprehensive list of data is ideally desired (site name, demographics, diagnoses, device, protocol, rating scales, perinatal outcome), any de-identified data is appreciated (please never provide names, treatment dates, or birth dates).

If you are willing to participate, please complete the information below.

Please note, submitted data will be owned by the CTMSS and data may be used for research publication.

Questions? Email info@clinicaltmssociety.org or drkoo@neurowellnessspa.com.

Sincerely,
The CTMSS Research Committee
1.Email(Required.)
2.TMS Device(Required.)
3.Rating Scales Utilized
Select all that apply.
(Required.)
4.Patient Demographics:
ID, age, race, gestational weeks at start of TMS, diagnoses, medications
(Required.)
5.Protocol and Efficacy:
rTMS protocol used, initial/subsequent MT values, and baseline/final rating scale scores
6.Side effects: Mother and infant
Apgar scores, gestational age at delivery, mode of delivery, weight, complications, NICU admission