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Behavioral Intervention

Exercise for Adverse Childhood Experiences (CTEC Trial)

N/A
Recruiting
Led By Erin Logue, PhD
Research Sponsored by University of Texas at Austin
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up one week before first acute exercise condition (baseline) and after 3 weeks of the chronic exercise condition or activity as usual
Awards & highlights

CTEC Trial Summary

This trial will study how exercise affects thinking in adults w/cog. complaints & childhood abuse/neglect. Participants tracked for 78 days in 5 parts w/lab exercises, symptom & neuropsych tests. 9-week exercise intervention or activity as usual outside of lab.

Who is the study for?
This trial is for middle-aged adults (40-60 years old) who experienced childhood abuse or neglect, have cognitive complaints but are medically healthy. They must speak English fluently and not have severe mental health issues, substance abuse problems, major medical conditions, or engage in high-intensity activities.Check my eligibility
What is being tested?
The study tests how different exercise intensities affect cognition over a period of up to 78 days. Participants will undergo initial assessments followed by acute exercises in the lab and a longer-term exercise regimen or their usual activity with regular cognitive testing.See study design
What are the potential side effects?
Since this trial involves moderate intensity exercise, potential side effects may include typical exercise-related discomforts such as muscle soreness, fatigue, shortness of breath during activity, and possibly joint pain.

CTEC Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one week before first acute exercise condition (baseline); after acute exercise condition on day 8; after acute exercise condition on day 15; and after 3 weeks, 6 weeks, and 9 weeks of the chronic exercise condition or activity as usual
This trial's timeline: 3 weeks for screening, Varies for treatment, and one week before first acute exercise condition (baseline); after acute exercise condition on day 8; after acute exercise condition on day 15; and after 3 weeks, 6 weeks, and 9 weeks of the chronic exercise condition or activity as usual for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change from baseline cognitive complaints (i.e., total number of complaints) at 3 weeks post-chronic exercise intervention.
Change from baseline cognitive complaints (i.e., total number of complaints) at 6 weeks post-chronic exercise intervention.
Change from baseline cognitive complaints (i.e., total number of complaints) at 9 weeks post-chronic exercise intervention.
+24 more
Secondary outcome measures
Change in total score on the Center for Epidemiological Studies Depression Scale Revised (CESD-R).
Change in total score on the Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5).

CTEC Trial Design

4Treatment groups
Experimental Treatment
Active Control
Group I: Chronic Exercise ModerateExperimental Treatment4 Interventions
9-weeks Moderate Intensity Exercise Day 36 (at 3 weeks) Assessments Day 57 (at 6 weeks) Assessments Day 78 (at 9 weeks) Assessments
Group II: Acute Exercise Moderate firstExperimental Treatment4 Interventions
Day 1 Assessments, Day 8 Moderate Intensity Exercise (followed by symptom measures and neuropsychological tests), Day 15 Light Intensity Exercise (symptom measures and neuropsychological tests)
Group III: Activity as UsualActive Control1 Intervention
9-week activity as usual Day 36 (at 3 weeks) Assessments Day 57 (at 6 weeks) Assessments Day 78 (at 9 weeks) Assessments
Group IV: Acute Exercise Light firstActive Control4 Interventions
Control Day 1 Assessments (symptom measures, neuropsychological tests, and cognitive complaints interview), Day 8 Light Intensity Exercise (followed by symptom measures and neuropsychological tests), Day 15 Moderate Intensity Exercise (symptom measures and neuropsychological tests)

Find a Location

Who is running the clinical trial?

University of Texas at AustinLead Sponsor
353 Previous Clinical Trials
81,210 Total Patients Enrolled
Erin Logue, PhDPrincipal InvestigatorUniversity of Texas at Austin

Media Library

Moderate Intensity Exercise (9 wks) (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05972265 — N/A
Adverse Childhood Experiences Research Study Groups: Chronic Exercise Moderate, Activity as Usual, Acute Exercise Moderate first, Acute Exercise Light first
Adverse Childhood Experiences Clinical Trial 2023: Moderate Intensity Exercise (9 wks) Highlights & Side Effects. Trial Name: NCT05972265 — N/A
Moderate Intensity Exercise (9 wks) (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05972265 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals younger than thirty years old qualified to participate in this experiment?

"As detailed in the eligibility requirements of this trial, participants must be between 40 and 60 years old."

Answered by AI

Are there any open opportunities to join this research trial?

"According to clinicaltrials.gov, this medical trial is currently inactive and no longer recruiting patients. The experiment was originally posted on September 1st 2023 and has since been edited for the last time on July 23rd of the same year. Luckily, there are 12 other trials that are presently searching for participants."

Answered by AI

Am I eligible to volunteer for this medical experiment?

"To qualify for this trial, the applicant must have experienced adverse childhood circumstances and be between 40-60 years old. We are looking to accept up to 34 participants in total."

Answered by AI
~20 spots leftby Dec 2024