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

NCT03487601 · ClinicalTrials.gov registry record · NA

Transcranial Direct Current Stimulation (tDCS) to Improve Fatigue and Cognitive Function

A NA study of Breast Cancer and Fatigue, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Completed
Registry status
NA
Development phase
3
Enrollment target
2
Study locations

NCT03487601: Completed NA study of Breast Cancer and Fatigue, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

NCT03487601 is a NA study of Breast Cancer and Fatigue that has completed, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 3 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (100% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03487601, a NA study of Breast Cancer and Fatigue, has completed, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

COMPLETED
Registry status
NA
Development phase
3 participants
Enrollment target
2
Study locations

Study Summary

This research is being done to determine whether transcranial direct current stimulation (tDCS) can improve fatigue and certain thinking skills in women with breast cancer receiving chemotherapy. Transcranial Direct Current Stimulation is a form of brain stimulation during which low amounts of electrical current are delivered to the brain using electrodes attached to the scalp. The idea of using electrical stimulation to affect neurological symptoms has been around for more than 100 years with the first reported use in 1801. Since the 1960s, tDCS has been used in research for a variety of reasons including stroke rehabilitation, memory enhancement and for depression. People aged 18 or older who are currently receiving chemotherapy with docetaxel and who are experiencing fatigue may join.

Primary Outcome

Evaluation of the feasibility of 5 consecutive days of tDCS in breast cancer patients receiving docetaxel-based chemotherapy. Feasibility will be evaluated by assessing the proportion of study participants who complete at least 4 of 5 days of the planned tDCS intervention (active or sham) during docetaxel-based chemotherapy. If \>80% of participants complete 4 of the 5 planned stimulation sessions, tDCS will be defined as feasible.

Conditions Studied

Interventions

  • OTHER transcranial direct current stimulation
  • OTHER sham transcranial direct current stimulation

Study Locations (2)

District of Columbia

  • Sibley Memorial Hospital - Washington D.C.

Maryland

  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins - Baltimore

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2017-12-12
Est. Completion 2019-02-16
Phase NA

What the finished NCT03487601 record still lists

NCT03487601 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (100% lower).

The record links to 2 conditions, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which transcranial direct current stimulation is the first listed.

NCT03487601 reports a single indexed study location in District of Columbia, Maryland.

Frequently Asked Questions

What is clinical trial NCT03487601 about?

NCT03487601 is a clinical study titled "Transcranial Direct Current Stimulation (tDCS) to Improve Fatigue and Cognitive Function". This research is being done to determine whether transcranial direct current stimulation (tDCS) can improve fatigue and certain thinking skills in women with breast cancer receiving chemotherapy. Transcranial Direct Current Stimulation is a form of brain stimulation during which low amounts of elec...

What is the current status of trial NCT03487601?

This trial is currently completed. It is a NA study. The enrollment target is 3 participants. The study started on 2017-12-12. Estimated completion is 2019-02-16.

What conditions does trial NCT03487601 study?

This clinical trial studies the following conditions: Breast Cancer, Fatigue.

What interventions are being tested in trial NCT03487601?

The interventions under investigation include: transcranial direct current stimulation (OTHER), sham transcranial direct current stimulation (OTHER).

Who is sponsoring clinical trial NCT03487601?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03487601 being conducted?

This trial has 2 study locations across District of Columbia, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Breast Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03487601's enrollment target sits among peer trials

3 1217th of 1224 higher than 6 of 1,224 other Breast Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Breast Cancer 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 registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03487601, the US trial registry maintained by the National Library of Medicine. NCT03487601 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.