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Completed

NCT Number: NCT00118014

Sertraline and Habit Reversal in the Treatment of Patients With Trichotillomania

The purpose of this study is to assess the extent of symptom remission in patients with trichotillomania following treatment with sertraline and/or behavior therapy.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Massachusetts General Hospital - OCD Clinic

Charlestown, Massachusetts, 02129, United States

About this study

The purpose of this study is to assess the extent of symptom remission in patients with trichotillomania following treatment with sertraline and/or behavior therapy.

Following entry into the study, subjects will undergo a washout period if they are currently taking a psychotropic medication (two weeks for psychotropic medications except for fluoxetine, which requires a four-week washout). Subjects will then be given a single-blind placebo for two weeks and assessed for symptom consistency.

Subjects will take sertraline or placebo in a double-blind design. Subjects will be assessed with the Hamilton Rating Scale for Depression (HAM-D-17), Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), Clinical Global Impressions Scale (CGI), Hair Pulling Scale (HPS), Trichotillomania (TTM) Impact Scale, Psychiatric Institute Trichotillomania Scale (PITS), National Institute of Mental Health (NIMH) Scale, and Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q) at the start of the washout period and at the end of week two in order to be randomized into the study. Subject randomization to a treatment arm will be based on the random table and in equal proportions.

Subject change scores will be assessed for the above scales, and change scores for the four different treatment groups will be assessed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients will have a DSM-IV diagnosis of TTM.
  • TTM symptoms for at least 4 months.
  • Scalp as primary site of hair pulling.
  • HPS score greater than or equal to 15 OR TTM Impact Scale score greater than 30.
  • Written informed consent.
  • Men or women aged 18-65 years old.
  • Females of childbearing potential must have a negative serum beta-HCG pregnancy test.

Exclusion criteria

  • Pregnant women or women of childbearing potential who are not using a medically accepted means of contraception.
  • Patients who, in the investigator's judgement, pose a serious suicidal or homicidal risk.
  • Serious or unstable medical illness including cardiovascular, hepatic, renal, respiratory, endocrine, neurologic, or hematologic disease. Patients on anticoagulant therapy.
  • History of seizure disorder.
  • Comorbid bipolar disorder, psychosis, organic mental disorder, or developmental disorder.
  • If there is a history of substance abuse, patients must be in remission at least 6 months.
  • Past trials of sertraline.
  • Currently being treated with behavioral therapy, specifically habit reversal training, for TTM.
  • Other medications for medical disorders that may interact with sertraline.

Treatment and study plan

Sertraline

Drug

Habit Reversal Training

Behavioral

Primary outcomes

  1. Clinical Global Impressions Scale change scores (week 2 versus 22)

    Time frame: Week 2 to 22

  2. Hair Pulling Scale change scores (week 0 versus 22)

    Time frame: Week 0 to 22

  3. TTM Impact Scale change scores (week 0 versus 22)

    Time frame: Week 0 to 22

  4. PITS (week 0 versus 22)

    Time frame: Week 0 to 22

  5. NIMH Scale (week 0 versus 22)

    Time frame: Week 0 to 22

Secondary outcomes

  1. HAM-D-17 (week 0 versus 22)

    Time frame: Week 0 to 22

  2. BDI (week 0 versus 22)

    Time frame: Week 0 to 22

  3. BAI (week 0 versus 22)

    Time frame: Week 0 to 22

  4. Q-LES-Q (week 0 versus 22)

    Time frame: Week 0 to 22

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Pfizer

Registry information

Important dates

Study start
2000
Primary completion
2004
Study completion
2004
First posted
Jul 11, 2005
Registry last updated
May 20, 2008

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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