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Completed

NCT Number: NCT03307070

Adapted Cognitive Behavioral Treatment for Depression in Patients With Moderate to Severe Traumatic Brain Injury

Cognitive behavioral therapy for major depressive disorder (MDD) was adapted for individuals with moderate to severe traumatic brain injury (TBI) (CBT-TBI). A structured, treatment manual was developed.

The primary aim is to evaluate the acceptability and tolerability of, and adherence to, CBT-TBI in a randomized waitlist-controlled, 12-week pilot trial (N=40).

The exploratory aim is to evaluate the potential efficacy of CBT-TBI for MDD in the randomized pilot trial (N=40) and possible moderators and mediators of outcome.

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Key information

Conditions

Major Depressive Disorder Brain Diseases Brain Injuries Brain Injuries, Traumatic Central Nervous System Diseases Craniocerebral Trauma Depressive Disorder Depressive Disorder, Major Mental Disorders Mood Disorders Nervous System Diseases Trauma, Nervous System Traumatic Brain Injury Wounds and Injuries

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

About this study

The primary aim of this study is to develop a highly acceptable, manualized treatment (CBT-TBI) for MDD in patients with moderate to severe TBI. Initial feasibility data from a small, open pilot will inform the randomized controlled trial. Primary analyses will examine feasibility and acceptability of the intervention. The investigators will then pilot test the efficacy of the intervention to reduce depressive symptoms (IDS-C) after 12 weeks compared to a waitlist control group.

The proposed study involves the following points of contact: (1) Obtaining informed consent and screening (may be broken up into multiple visits), (2) biweekly clinician assessments of depressive and neuropsychiatric symptoms (weeks 2, 4, 6, 8, 10), (3) weekly self-report assessments of depressive symptoms for those receiving the intervention, (4) 12 weekly individual CBT-TBI sessions for those randomized to the intervention, (5) a comprehensive assessment at week 12 (primary endpoint), which includes the neuropsychological battery, and (6) a 3-month follow-up assessment for those who received the intervention. The week 12 visit can be split into two parts, with the neuropsychological assessment occurring during the second part, in order to accommodate subjects' potential limitations due to fatigue. Procedures for this study were all conducted remotely after March 17, 2020.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adults aged 18 and older
  • English language proficiency
  • Ability to provide written, informed consent; OR consent provided by legally authorized representative with assent from subject
  • Ability to see and hear (hearing or visual loss cannot impair ADLs or in-room conversation)
  • Has access to a smartphone/tablet/computer with internet and video capabilities for virtual sessions
  • Having been hospitalized for moderate to severe TBI that occurred at least 3 months prior to study entry
  • Meeting ANY ONE of the following severity criteria, as documented in electronic medical record (EPIC) or available outside records:
  • GCS 3-12 with GCS motor score ≤ 5 within 4 hours after injury
  • GCS 3-12 with GCS motor score =6 within 4 hours after injury AND documented intracranial abnormalities on imaging
  • GCS 13-15 within 4 hours after injury AND documented intracranial abnormalities on imaging
  • Loss of consciousness (LOC) > 30 min.
  • Post-traumatic amnesia (PTA) > 24 hours
  • Out of PTA at the time of enrollment (GOAT>75)
  • Clinically significant depressive symptoms: meets criteria for Major Depressive Episode on the MINI or has a total score ≥ 23 on the Inventory of Depressive Symptomatology - Clinician rated (IDS-C)

Exclusion criteria

  • Uncontrolled medical illness
  • Behavioral dyscontrol, defined as the presence of verbally or physically aggressive behavior in the past month, as evidenced in medical records, pre-screening interviews, or observed by any study staff
  • Presents with PTSD as the primary diagnosis, as determined by a clinician
  • Substance use disorder, moderate or severe, within the past 6 months
  • Has bipolar disorder, a primary psychotic disorder or current psychotic symptoms, or acute suicidality or homicidality
  • Currently receiving regular (≥ 2 times/ mo.) psychosocial treatment for depression
  • Has participated in CBT for depression within the past 6 months
  • Individuals with history of dementia or severe cognitive impairment that is not related to TBI (e.g., cognitive impairment requiring assistance with basic activities of daily living, such as getting ready in the morning)

Treatment and study plan

Cognitive Behavioral Therapy for individuals with TBI

Behavioral

Cognitive Behavioral Therapy for depression that has been adapted for a population who has experienced a moderate to severe Traumatic Brain Injury. This is a 12 week long treatment for depression with weekly visits that challenges negative thoughts and behaviors. This version has been specifically developed for the study to account for specific cognitive needs of individuals who have experienced a moderate to severe TBI.

Waitlist Control

Other

Participants will be randomized to a waitlist. They will attend biweekly study sessions for 12 weeks to track progress, but will receive their treatment as usual.

Primary outcomes

  1. Feasibility - retention/completion rates

    Time frame: 12 weeks

    For examining the feasibility of treatment with CBT-TBI, descriptive analyses will be conducted to assess participants' retention/completion rates across study visits.

  2. Feasibility - drop out rates

    Time frame: 12 weeks

    For examining the feasibility of treatment with CBT-TBI, descriptive analyses will be conducted to assess participants' drop-out rates across study visits.

  3. Feasibility - randomization, recruitment rates

    Time frame: 12 weeks

    For examining the feasibility of treatment with CBT-TBI, descriptive analyses will be conducted to assess rate of recruitment and randomization (number randomized/number consented).

  4. Acceptability - satisfaction with treatment

    Time frame: 12 weeks

    Descriptive analyses will be conducted to assess participants' satisfaction with CBT-TBI (Satisfaction with Therapy and Therapist Scale - Revised).

Secondary outcomes

  1. Efficacy - Treatment Response [Inventory of Depressive Symptomatology - Clinician Rated (IDS-C)] (Exploratory Aim)

    Time frame: 12 weeks

    The IDS-C is a 30-item clinician rated scale that assesses severity of depression. Scores range from 0 to 84, with higher scores indicative of greater depression severity.

    Descriptive analyses will be performed for percentage of responders (defined as 50% improvement on the IDS-C total) and remitters (≤6 on IDS-C total) at the end of treatment. The percent of responders and remitters in each group will be computed in order to estimate an effect size for a larger trial.

  2. Efficacy - Treatment Response [Inventory of Depressive Symptomatology - Clinician Rated (IDS-C)] (Exploratory Aim)

    Time frame: 12 weeks

    The IDS-C is a 30-item clinician rated scale that assesses severity of depression. Scores range from 0 to 84, with higher scores indicative of greater depression severity.

    Change in depressive severity (IDS-C total) scores from baseline to post-treatment will also be analyzed.

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Spaulding Rehabilitation Hospital

Registry information

Important dates

Study start
2017
Primary completion
2022
Study completion
2022
First posted
Oct 11, 2017
Registry last updated
Apr 10, 2023

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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