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Completed

NCT Number: NCT03627078

Motor Interference Therapy For Traumatic Memories

The aim of the study is to compare the effect of motor interference therapy (TIM) to reduce the intensity of discomfort (distress) generated by a traumatic memory compared to a relaxation control maneuver, immediately after the intervention, a week, a month and six months after intervention.

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Instituto Nacional de Neurologia Y Neurocirugia Mvs

Mexico City, 14269, Mexico

About this study

The investigators treated 10 patients with autobiographical traumatic memories using finger tapping tasks, (Motor Interference Therapy <TIM>)in a pilot study with amazing results and a solid size effect. The investigators decided to challenge the intervention using a control task (Jacobson´s progressive relaxation exercises) The hypothesis consists in achieving a 30% reduction of the distress, (measured with Visual Analogue Scale) by using TIM compared with the control task. Patients with traumatic memories will be enrolled in to one of two treatment modalities. The first group will receIve motor interference therapy and the second group will receive a control task (relaxation exercises). Both groups will be assessed using the Spanish version of the PTSD Symptom Severity Scale-Revised (EGS-R), the visual analogue scale (EQ-VAS) from EuroQol 5D (EQ-5D), and a simple visual-analogue scale (VAS) immediately after, a week after, a month after and six months after the treatment for follow up.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients older than 16 years
  • Spanish as a native language
  • Give written informed consent
  • having at least 1 traumatic memory causing distress

Exclusion criteria

  • Neurological or psychiatric disorders that affect the capacity of verbal comprehension and judgment, such as dementia, psychosis, mental retardation or other cognitive alteration that does not allow them to perform the tasks indicated in the TIM or SHAM
  • History of recent substance abuse
  • Patients with significant hearing loss or some other hearing impairment

Treatment and study plan

motor interference therapy

Other

Other names: TIM

Relaxation exercises

Other

In a top-down sequence, beginning with the upper body and proceeding to the lower parts. patients contract and relax a specific muscle group following the instructions given by the audio track. We use a shorter version that excludes the legs because of the time.

Other names: Jacobson´s progressive relaxation

Primary outcomes

  1. Change in Visual Analogue Scale (EVA)

    Time frame: baseline, immediately, 1 week, 1 month, 6 months

    measures the distress related to traumatic memories in 1-10

Secondary outcomes

  1. Spanish version of the PTSD Symptom Severity Scale-Revised (EGS-R)

    Time frame: baseline, 1 week, 1 month, 6 months

    Posttraumatic stress disorder scale

  2. visual analogue scale (EQ-VAS) from EuroQol 5D (EQ-5D)

    Time frame: baseline, 1 week, 1 month, 6 months

    as a gauge of health-related quality of lif

Sponsors and collaborators

Lead sponsor

El Instituto Nacional de Neurologia y Neurocirugia Manuel Velasco Suarez

Other

Registry information

Official study title

The Effect of Motor Interference Therapy In Traumatic Memories: A Controlled Clinical Trial

Acronym: TIMCO

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Aug 13, 2018
Registry last updated
Jul 29, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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