CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 51 enrolled
Drug / intervention
tDCS +2 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03178903
NCT03178903N/ACompleted

tDCS for Increasing Exercise Adherence in Individuals With Elevated Depressive Symptoms

Butler Hospital·interventional·Posted Jun 7, 2017·Updated Feb 27, 2023

In Brief

A clinical study evaluating tDCS, Sham tDCS, and 1 other intervention for Depression and Physical Activity. Completed, enrolled 51 participants across 1 site.

Detailed Summary

The purpose of this study is to examine the efficacy of tDCS (transcranial direct current stimulation) for increasing exercise adherence among low active individuals with elevated depressive symptoms. The investigators expect that this project will contribute much needed knowledge about the role that tDCS can play in changing the affective experience of exercise.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJun 7, 2017
Enrollment StartFeb 1, 2017
Primary CompletionDec 31, 2019
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 9.1 years ago

Interventions

tDCSother

Participants in transcranial direct current stimulation (tDCS) will receive tDCS over the dorsal-lateral prefrontal cortex for 20 minutes, 3 times per week for 8 weeks.

Sham tDCSother

Participants in sham transcranial direct current stimulation (tDCS) will receive shame tDCS over the dorsal-lateral prefrontal cortex for 20 minutes, 3 times per week for 8 weeks.

Aerobic Exercise (AE)behavioral

Participants will engage in supervised, 30-minute bouts of moderate-intensity exercise 3x/week for 8 weeks.