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Borderline Personality DisorderRESTNCT04507308

Real-time Experiences With Sleep Training Study

A study testing Single-session sleep intervention drawn from principles of the TSC-youth protocol in people with Borderline Personality Disorder and Sleep Disturbance, run by University of Utah at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Borderline personality disorder (BPD) is a serious mental illness that often first emerges in adolescence. Effective treatments are typically expensive, lengthy, and intense (e.g., Dialectical Behavior Therapy). Thus, setting individuals up for treatment success is extremely important. Read more about this study

Who is it for?
Ages 13 to 18 years
What is being tested?
Single-session sleep intervention drawn from principles of the TSC-youth protocol
Could I receive a placebo?
No, everyone receives an active treatment
How many people
57 participants
Where
1 siteCanada
Study dates
1 Jun 2024to 21 Jun 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 13 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Youth between 13 and 18 years of age
  • 3+ clinically impairing symptoms of borderline personality disorder as determined via screening interview
  • Parent available to complete informant-report and accompany participant to sleep intervention session
  • Participant has a cellular phone or reliable access to a computer to complete ecological momentary assessment protocol

Who cannot join

  • Participants without English language proficiency will be excluded as the study requires verbal and written components delivered exclusively in English.
  • Participants with fewer than 3 clinically impairing BPD symptoms will be excluded from the study.
  • We will exclude adolescents who present with an intellectual disability or have a schizophrenia spectrum diagnosis.
  • Participants who do not have a parent/caregiver available to attend the virtual intervention session will also be excluded from the study.
  • Participants without access to a personal cellular phone or reliable access to a computer with internet will be excluded.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • University of Western Ontario Westminster Hall

    London, Ontario, N6G 2M1

Other trials in Canada

About this study

Borderline personality disorder (BPD) is a serious mental illness that often first emerges in adolescence. Effective treatments are typically expensive, lengthy, and intense (e.g., Dialectical Behavior Therapy). Thus, setting individuals up for treatment success is extremely important. Disrupted sleep is closely linked to many BPD symptoms (e.g., moodiness, impulsivity, interpersonal problems), and people with BPD have a range of sleep-related problems. Importantly, sleep problems may make BPD symptoms worse, longer lasting, and also interfere with learning new skills in treatment. Understanding sleep problems in BPD may help create better interventions, as most therapies for BPD do not currently address sleep difficulties. Although approaches like Cognitive Behaviour Therapy for insomnia (CBT-I) and the Youth version of the Transdiagnostic Sleep and Circadian Intervention (TSC-Youth) work well with many populations, scientists don't yet know if youth with BPD features can tolerate a sleep-focused intervention. The investigators will recruit youth between ages 13 and 18 who have 3 or more clinically impairing BPD symptoms from the Salt Lake City community, via chart review, and via clinician referrals. They will also recruit a parent to report on their child's sleep patterns, mental health symptoms, and accompany youth to an intervention session. Participants will complete diagnostic interviews and a range of surveys to assess their current functioning (e.g., sleep, mental health, BPD symptoms). Investigators will also ask youth to report on their BPD symptoms multiple times per day in real time and track their sleep at night for a 10-day period. Participants will also wear a headband to track their brain waves while they sleep. After an initial 10-day monitoring period, youth participants will receive a brief, single-session sleep intervention with their parent using materials from the TSC-Youth protocol. Adolescents will be asked to follow a sleep plan created during their visit for three weeks before completing another 10 days of assessment. Participants will complete a follow-up survey battery upon completion of the second real-time survey protocol, and also be invited to complete surveys one-month post intervention. The investigators hypothesize that day-to-day variability in sleep will influence BPD symptom presentation, and vice versa. They also hypothesize that our intervention will improve sleep quantity/quality among an at-risk sample, and may be associated with decreased BPD symptoms relative to baseline.

Read the detailed description

Borderline personality disorder (BPD) is a persistent and profoundly impairing mental disorder characterized by interpersonal turmoil, severe emotion dysregulation, and impulsivity(1). BPD often first manifests in adolescence(2) and even subthreshold levels of symptoms are associated with significant psychosocial morbidity(3). Approximately 69% to 80% of persons with this condition engage in self-injurious behavior, and as many as 9% die by suicide(4-5). Although efficacious treatment approaches have been developed (e.g., Dialectical Behavior Therapy [DBT];6), they are typically expensive, lengthy, and intensive. Identifying methods for optimizing BPD treatment and prevention is an urgent public health priority.

Disrupted sleep is closely linked to defining characteristics of BPD such as higher sensitivity and reactivity to stress, behavioral impulsivity, interpersonal dysfunction, and poor emotion regulation(7). Studies have documented a range of sleep disturbances among BPD samples, and demonstrated that sleep problems are not better accounted for by concomitant depression or other psychiatric disorders(7-9). Importantly, sleep problems may worsen BPD symptom course and chronicity(10-11), heighten risk of suicide(12-13) and self-harm(14), and interfere with cognitive processes that are vital to behavioral intervention (e.g., memory consolidation, and attentional processes; 15). A greater understanding of sleep disturbance in BPD may help enrich treatment protocols, which currently place limited emphasis on sleep difficulties(11). Although approaches like Cognitive Behaviour Therapy for insomnia (CBT-I) and the Youth version of the Transdiagnostic Sleep and Circadian Intervention (TSC-Youth) are effective with many populations(16), it is currently unknown whether sleep-focused interventions can be tolerated or followed adherently by youth with BPD features (who are often extremely dysregulated across affective, interpersonal, and behavioral domains).

Objectives: 1) To assess transactional relations of sleep, interpersonal stressors, affect, impulsive behaviors, and self-harm among youth with BPD features (N = 57); 2) To assess the effects of a brief sleep intervention on subsequent sleep quality (primary outcome) and BPD symptoms (secondary outcome). This pilot study will establish recruitment feasibility, determine the acceptability and efficacy of a sleep-focused intervention among adolescents with BPD features, and provide crucial preliminary data to support future grants.

Methodology. The investigators will use a pre-post intervention design with 2 assessments. Changes in BPD symptoms, self-reported sleep quality, and ambulatory monitoring of electroencephalogram (EEG) during sleep, will be assessed approximately 30 days post-treatment. Two 10-day EMA protocols (one prospective and one post-intervention) will provide data for transactional analyses.

Participants: Adolescents ages 13-18 (N=57) will participate with a parent.

Recruitment will be conducted through chart review at the Huntsman Mental Health Institute, physician and therapist referrals, and ethics-approved media advertisements and fliers. Interested participants (and a parent) will complete a brief telephone or Zoom screen to determine initial eligibility and schedule two virtual visits.

Research Protocol:

  1. Phone Screening/Eligibility: -Parental verbal consent for phone screen and Youth verbal assent for phone screen
  • Brief interview to determine eligibility: McLean Screening Interview
  • Schedule virtual visit 1
  1. At visit 1, perform consent/assent and sign forms via electronic signature on REDCap; see "Parental Permission and Authorization Document" and "Assent")

Virtual Visit 1 via Zoom

  • Pre-visit risk assessment with youth (UWRAP)
  • Interviews:
  • The Childhood Interview for Borderline Personality Disorder
  • Lifetime Suicide Attempt Self-Injury Interview (L-SASII)
  • Means-End Problem-Solving Task (MEPS)
  • Schedule Sleep Band pick-up-participants to pick up on campus or coordinate other arrangements, as needed (e.g., mail).
  • End-of-visit risk assessment with youth
  1. Baseline Questionnaires:
  • Send parents and youth measures via email for electronic completion on REDCap:

Youth questionnaires:

  • Demographic Questionnaire
  • The Difficulties in Emotion Regulation Scale Short Form (DERS-SF)
  • Adolescent Sleep Hygiene Scale
  • Borderline Personality Features Scale for Children-11(BPFS-C-11)
  • PROMIS Pediatric Sleep Disturbances SF8
  • PROMIS Pediatric Sleep Related Impairment SF8
  • Self-Concept and Identity Measure (SCIM)
  • Adolescent Sleep Wake Scale - 10 item version
  • Urgency, Premeditation (lack of), Perseverance (lack of), Sensation Seeking, Positive Urgency, Impulsive Behavior Scale Short form (UPPS-P)
  • Items from the Sleep Practices and Attitudes Questionnaire

Parent-Report:

  • Demographic Questionnaire
  • PROMIS Pediatric Sleep Disturbances Parent Proxy SF8
  • PROMIS Pediatric Sleep Practices Parent Proxy
  • Sleep Disturbance Scale for Children
  • PROMIS Pediatric Sleep Related Impairment Parent Proxy SF4
  • Child Behavior Checklist (CBCL)
  • Participants receive/pick-up sleep band ~
  • Provide psychoeducation and instructions on wearing sleep band and completing EMA protocol
  • Schedule visit 2 (intervention visit)
  1. Ecological momentary assessment (EMA) and EEG Protocol 1 (10 days):
  • EMA assessments are collected 5 times per day. Upon waking, participants report bed time and wake time for calibration with sleep EEG data
  • Each daily survey assesses current mood, sleep, and BPD symptoms since the last prompt (e.g., perceived emotional control/dyscontrol, emotional lability, interpersonal conflict, impulsive behavior, dissociation, self-harm urges/behaviors; see attached EMA protocol).
  • Research staff monitor EMA responses each day.
  • When responses during the EMA protocol indicate imminent risk of suicide or self-injury, 988 and SafeUT contact information automatically display on participants' smart phone, and research staff immediately receive an automated e-mail. Research staff are able to log into REDCap to view participants' responses, and may contact the participant by text or telephone for risk assessment and safety planning. Appropriate intervention or follow-up care will be arranged. In cases of immediate safety risk, the research team define a feasible safety plan with the participant (this may include other members in the participants' network and/or crisis intervention services and emergency care). If child abuse or neglect is disclosed, the alleged abuse will be reported to DCFS. During the consent process, all participants will be informed of limits to confidentiality and our legal obligations to report dangerous situations. EMA protocols of similar duration and assessment frequency have been successfully conducted with individuals at risk for self-harm with excellent participant compliance rates (21-23).
  1. ~ Participant returns sleep band ~
  2. Virtual visit 2 via Zoom
  • Pre-visit risk assessment
  • Together, youth and parent watch a video providing psychoeducation about sleep
  • Youth will receive a sleep-focused skills training session with their parent:
  • A clinical psychology graduate student or Dr. Kaufman completed the following handouts from the TSC Youth protocol (an established, evidence-based sleep intervention for adolescents) in collaboration with the participant and their parent:
  • "Functional Analysis"
  • "Improving Your Sleep Summary"
  • "My Sleep Goals"
  • "Rise-up checklist"
  • "Wind-down handout"
  • "Stimulus Control"
  • Participants will be asked to practice the skills they have learned for the following month and be provided digital copies of their worksheets to support their unique sleep plan.
  • End-of-visit risk assessment ~ 3-to-4-week period where youth implement and get accustomed to their new sleep plan ~
  1. Sleep headband band pick-up (on campus)
  2. Post-EMA and EEG Protocol 2 (10 days; 3-4 weeks post-intervention)
  • EMA assessments will proceed as they did for protocol 1 (i.e., 5 times per day), with additional prompts to assess sleep plan/skill usage. ~Research staff monitored EMA responses daily for compliance and safety as described above.
  1. Sleep headband drop-off (on campus)
  2. Post-test Questionnaires:
  • Send parents and youth measures via email for electronic completion on REDCap:

Youth:

  • DERS-SF
  • Adolescent Sleep Hygiene Scale
  • BPFS-C-11
  • PROMIS Pediatric Sleep Disturbances SF8
  • PROMIS Pediatric Sleep Related Impairment SF8
  • SCIM
  • Adolescent Sleep Wake Scale - 10 item version
  • UPPS-P
  • Items from the Sleep Practices and Attitudes Questionnaire

Parents:

  • PROMIS Pediatric Sleep Disturbances Parent Proxy SF8
  • PROMIS Pediatric Sleep Practices Parent Proxy
  • Sleep Disturbance Scale for Children
  • PROMIS Pediatric Sleep Related Impairment Parent Proxy SF4 ~Questionnaires need to be completed no later than 1 week after 2nd EMA protocol.~
  1. Payment given for EMA electronically (emailed) after sleep band is returned undamaged
  2. 1-Month Follow-up
  • Participants will be emailed questionnaires 1-month following completion of their second EMA protocol.
  • Youth emailed:
  • DERS-SF
  • Adolescent Sleep Hygiene Scale
  • BPFS-C-11
  • PROMIS Pediatric Sleep Disturbances SF8
  • PROMIS Pediatric Sleep Related Impairment SF8
  • SCIM
  • Adolescent Sleep Wake Scale - 10 item version -Parents emailed:
  • PROMIS Pediatric Sleep Disturbances Parent Proxy SF8
  • PROMIS Pediatric Sleep Practices Parent Proxy
  • Sleep Disturbance Scale for Children
  • PROMIS Pediatric Sleep Related Impairment Parent Proxy SF4
Being tested
Single-session sleep intervention drawn from principles of the TSC-youth protocol
Keywords
ecological momentary assessment, electroencephalogram, Transdiagnostic Sleep and Circadian Intervention Youth
Medical subject headings
Borderline Personality Disorder, Parasomnias

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Single-session sleep intervention drawn from principles of the TSC-youth protocolBehavioural

    We are providing participants psychoeducation on sleep and will be going over several handouts from the Youth version of the Transdiagnostic Sleep and Circadian Intervention (TSC-Youth) to improve sleep.

Study groups in NCT04507308
Study groupRoleWhat they receive
Transdiagnostic Sleep and Circadian InterventionExperimentalAll participants will undergo baseline assessment and then complete a brief, single-session sleep-focused intervention based on psychoeduation and handouts from the Youth version of the Transdiagnostic Sleep and Circadian Intervention (TranS-C-Youth).
Receives: Behavioral: Single-session sleep intervention drawn from principles of the TSC-youth protocol

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Sleep improvement

    Change from baseline sleep data (self- and informant-report, electroencephalogram data during sleep, and ecological momentary assessment data) to post-intervention data.

    Measured: Baseline data will be collected over the course of a 10 day period (including ecological momentary assessment data) and compared to data collected over a second 10 day window one-month post intervention.

  2. Change in borderline personality disorder symptoms

    Change in participants' BPD symptoms from baseline (assessed via diagnostic interview and a 10-day ecological momentary assessment protocol) to one-month post-intervention (via a second 10-day ecological momentary assessment protocol).

    Measured: Baseline data will be collected over the course of a 10 day period (including ecological momentary assessment data) and compared to data collected over a second 10 day window one-month post intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Aug 2020
  2. Study start1 Jun 2024
  3. Primary completion21 Jun 2026
  4. Study completion21 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
All participants are completing the same study procedure.
Masking
None (open label)
Enrolment
57 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04507308
Sponsor's protocol ID
00170667
Other IDs
31556
Acronym
REST
Status last verified
Aug 2026
First submitted
5 Aug 2020
Last updated
7 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified data may be shared with scientific collaborators in the future. Given the sensitive nature of study data, and that our sample includes vulnerable youth, we will not provide unrestricted access to all study variables. A subset of de-identified questionnaire, interview, and psychophysiological data may be made available by request. Researchers interested in more sensitive data (e.g., demographic variables that, in combination, could increase the odds of participant identification \[age, sex, race, ethnicity, gender identity, and sexual orientation\]) can request variables of interest from the principle investigator, and will be asked to complete a plan for data security.

Publications

  • American Psychiatric Association, & American Psychiatric Association. DSM-5 Task Force. (2013). Diagnostic and statistical manual of mental disorders: DSM-5. (Fifth edition.). Washington, DC: American Psychiatric Association.

  • Kaess M, Brunner R, Chanen A. Borderline personality disorder in adolescence. Pediatrics. 2014 Oct;134(4):782-93. doi: 10.1542/peds.2013-3677. Epub 2014 Sep 22.

    PubMed 25246626
  • Zimmerman M, Chelminski I, Young D, Dalrymple K, Martinez J. Is dimensional scoring of borderline personality disorder important only for subthreshold levels of severity? J Pers Disord. 2013 Apr;27(2):244-51. doi: 10.1521/pedi.2013.27.2.244.

    PubMed 23514187
  • Soloff P, Lis J, Kelly T, Cornelius J & Ulrich R (1994). Self-mutilation and suicidal behavior in borderline personality disorder. Journal of Personality Disorders, 8, 257-267. doi: 10.1521/pedi.1994.8.4.257

  • Zanarini MC, Frankenburg FR, Hennen J, Reich DB, Silk KR. The McLean Study of Adult Development (MSAD): overview and implications of the first six years of prospective follow-up. J Pers Disord. 2005 Oct;19(5):505-23. doi: 10.1521/pedi.2005.19.5.505.

    PubMed 16274279
  • Linehan, M. M. (1993). Cognitive-behavioral treatment of borderline personality disorder. New York: Guilford Press.

  • Winsper C, Tang NK, Marwaha S, Lereya ST, Gibbs M, Thompson A, Singh SP. The sleep phenotype of Borderline Personality Disorder: A systematic review and meta-analysis. Neurosci Biobehav Rev. 2017 Feb;73:48-67. doi: 10.1016/j.neubiorev.2016.12.008. Epub 2016 Dec 15.

    PubMed 27988314
  • Bastien CH, Guimond S, St-Jean G, Lemelin S. Signs of insomnia in borderline personality disorder individuals. J Clin Sleep Med. 2008 Oct 15;4(5):462-70.

    PubMed 18853705
  • Benson KL, King R, Gordon D, Silva JA, Zarcone VP Jr. Sleep patterns in borderline personality disorder. J Affect Disord. 1990 Apr;18(4):267-73. doi: 10.1016/0165-0327(90)90078-m.

    PubMed 2140379
  • Plante DT, Frankenburg FR, Fitzmaurice GM, Zanarini MC. Relationship between sleep disturbance and recovery in patients with borderline personality disorder. J Psychosom Res. 2013 Apr;74(4):278-82. doi: 10.1016/j.jpsychores.2013.01.006. Epub 2013 Feb 11.

    PubMed 23497827
  • Selby, E.A., Ribeiro, J.D., Joiner Jr., T.E. (2013). What dreams may come: Emotional cascades and nightmares in borderline personality disorder. Dreaming, 23, 126.

  • Balestrieri M, Rucci P, Sbrana A, Ravani L, Benvenuti A, Gonnelli C, Dell'osso L, Cassano GB. Lifetime rhythmicity and mania as correlates of suicidal ideation and attempts in mood disorders. Compr Psychiatry. 2006 Sep-Oct;47(5):334-41. doi: 10.1016/j.comppsych.2006.01.004. Epub 2006 Apr 21.

    PubMed 16905394
  • Winsper C, Tang NK. Linkages between insomnia and suicidality: prospective associations, high-risk subgroups and possible psychological mechanisms. Int Rev Psychiatry. 2014 Apr;26(2):189-204. doi: 10.3109/09540261.2014.881330.

    PubMed 24892894
  • Semiz UB, Basoglu C, Ebrinc S, Cetin M. Nightmare disorder, dream anxiety, and subjective sleep quality in patients with borderline personality disorder. Psychiatry Clin Neurosci. 2008 Feb;62(1):48-55. doi: 10.1111/j.1440-1819.2007.01789.x.

    PubMed 18289141
  • Curcio G, Ferrara M, De Gennaro L. Sleep loss, learning capacity and academic performance. Sleep Med Rev. 2006 Oct;10(5):323-37. doi: 10.1016/j.smrv.2005.11.001. Epub 2006 Mar 24.

    PubMed 16564189

Questions about this trial

What is this clinical trial studying?

A study testing Single-session sleep intervention drawn from principles of the TSC-youth protocol in people with Borderline Personality Disorder and Sleep Disturbance, run by University of Utah at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Sleep improvement (time frame: Baseline data will be collected over the course of a 10 day period (including ecological momentary assessment data) and compared to data collected over a second 10 day window one-month post intervention.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04507308, which also lists 23 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Aug 2026.

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