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Feasibility and Acceptability of Cognitive Behavioral Therapy for Chronic Insomnia in a Primary Care

Primary Purpose

Insomnia Chronic

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cognitive behavioral therapy for insomnia
Sponsored by
Balearic Islands Health Service (Ibsalut)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia Chronic focused on measuring primary care, cognitive behavioral therapy, clinical trial, feasibility-pilot study

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • 18 to 65 years-old
  • Diagnoses of chronic insomnia according to the Insomnia Severity Index (ISI equal or higher than 8) and had insomnia longer than 3 months;
  • Did or did not use a hypnotic medication.

Exclusion criteria:

  • Clinical diagnosis of secondary insomnia or another sleep disorder, such as restless legs syndrome, parasomnia, or alterations of the circadian rhythm (e.g., due to shift work)
  • Use of a medication that could produce sleep alterations
  • Severe psychiatric disorder; depression (HADS score ≥ 8) or diagnosis of major depression in the clinical records
  • Suicide attempt
  • Use of an antidepressant or anti-psychotic medication
  • Alcohol or drug abuse during the last year
  • Reception of another CBT-i
  • Sleep apnea
  • Dementia or presence of a cognitive deficit (Mini Mental State Evaluation score lower than 23)
  • Neurodegenerative or oncological disease with poor prognosis
  • Mental or physical incapacities that impeded participation in interviews
  • Acute or chronic pain secondary to a rheumatic disease or another untreated chronic disease
  • Pregnancy
  • Participation in a previous clinical trial in the participating health centers

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Cognitive behavioral therapy (CBT)

    Usual care

    Arm Description

    5 sessions of Cognitive behavioral therapy for insmonia and an extra session for benzodiazepine withdrawal (if necessary). The CBT-i included sleep hygiene counseling, stimulus control, cognitive restructuring, relaxation techniques, and benzodiazepine therapy or withdrawal

    Usual care from GPs or nurses

    Outcomes

    Primary Outcome Measures

    Acceptability of the training of PCPs
    Satisfaction with training content and its ability to provide sufficient training measured though 2 nominal groups with a previous script

    Secondary Outcome Measures

    Feasibility of the intervention
    Adequacy of sessions in terms of content, duration and number, fitting in PCPs agenda and patients acceptance.
    Feasibility of the study design
    Number of patients eligible identified and included, number of PCP randomized, number of patients followed up,completion of follow up and adherence to intervention sessions.
    Intervention Effectiveness: Sleep
    The Pittsburgh Sleep Quality Index (PSQI) is a 19-items self reported questionnaire that assesses 7 clinical components of sleep quality. Each item is rated on 0 to 3 point scale in which 0 is equal to not in the past month and 3 is equal to 3 or more times a week, with a global score range from 0 to 21. A cut off score of 5 has shown to discriminate between good and bad sleepers.
    Intervention Effectiveness:Anxiety
    The Hospital Anxiety and Depression Scale (HADS) measures anxiety and depression levels in the preceding week. It is 14-item self-report scale with two 7-item anxiety or depression subscales. Each item scores from 0 to 3 point scale giving maximum subscale scores of 21. Patients with scores >10 are considered to have morbidity, between 8 and 10 as borderline cases and <8 absence of relevant

    Full Information

    First Posted
    August 28, 2020
    Last Updated
    September 21, 2020
    Sponsor
    Balearic Islands Health Service (Ibsalut)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04565223
    Brief Title
    Feasibility and Acceptability of Cognitive Behavioral Therapy for Chronic Insomnia in a Primary Care
    Official Title
    Asessing the Feasibility and Acceptability of a Cluster Randomized Study of Cognitive Behavioral Therapy for Chronic Insomnia in a Primary Care.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    September 1, 2014 (Actual)
    Primary Completion Date
    April 1, 2015 (Actual)
    Study Completion Date
    November 1, 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Balearic Islands Health Service (Ibsalut)

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This pilot-feasibility study of a cluster parallel randomized design comparing CBT-i against usual care (UC) was performed at two primary health care centers in Majorca, Spain. Patients were included if they were 18 to 65 years-old; had diagnoses of chronic insomnia according to the Insomnia Severity Index (ISI more than 8) and had insomnia longer than 3 months; and did or did not use a hypnotic medication. 25 GPs and nurses and 32 patients were randomly allocated to two groups: The outcome of the trial was improving the quality of sleep. Other primary outcomes on feasibility and applicability of the intervention were collected through nominal groups. Description of usual care was described through previous studies. Moreover we assessed recruitment process, compliance with the intervention sessions, and patient's retention.
    Detailed Description
    Objectives The primary objectives of this pilot-feasibility study were: To design and adapt a brief CBT-i intervention to be provided by PCPs for the treatment of chronic insomnia in individuals who are 18 to 65 years-old. To define usual care (UC) for the treatment of chronic insomnia provided by PCPs as a comparative intervention (control group). To assess the training activities for the CBT-i intervention by determining GPs' and nurses' satisfaction with the content and applicability of the intervention. To determine the acceptability of the intervention by GPs and nurses. To assess PCPs and patient recruitment, follow-up, and adherence to the intervention The secondary objective was to assess the quality of sleep in patients after 3 months of the CBT-i. Methods Design This pilot-feasibility study of a cluster parallel randomized design comparing CBT-I against usual care (UC) was performed from September 2014 to April 2015 at two primary health care centers of Majorca (Spain) with 56,000 registered inhabitants. Collection of information and follow up Intervention The CBT-i intervention was developed by two family physicians (IT and CV) and two psychologists (ET and MRP-P). First, a review of the literature on the use of CBT-i was performed, with a focus on interventions applied in primary care. After the literature review, the CBT-i created by Morin [24] was adapted to our setting, in which there were fewer sessions and shorter sessions. The CBT-i included sleep hygiene counseling, stimulus control, cognitive restructuring, relaxation techniques, and benzodiazepine therapy or withdrawal (when needed). To conduct the intervention, guidelines for GPs and nurses and graphic and written materials for patients (sleep diary, registry of behavior habits, and cognitive problems) were developed. Usual care The usual treatment for persistent insomnia in a primary care setting was previously described in two cross-sectional studies performed by general practitioners and family nurses of the Primary Care Majorca Department during 2011 and 2015

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Insomnia Chronic
    Keywords
    primary care, cognitive behavioral therapy, clinical trial, feasibility-pilot study

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    32 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Cognitive behavioral therapy (CBT)
    Arm Type
    Experimental
    Arm Description
    5 sessions of Cognitive behavioral therapy for insmonia and an extra session for benzodiazepine withdrawal (if necessary). The CBT-i included sleep hygiene counseling, stimulus control, cognitive restructuring, relaxation techniques, and benzodiazepine therapy or withdrawal
    Arm Title
    Usual care
    Arm Type
    No Intervention
    Arm Description
    Usual care from GPs or nurses
    Intervention Type
    Behavioral
    Intervention Name(s)
    Cognitive behavioral therapy for insomnia
    Intervention Description
    is a multicomponent intervention which focuses on cognitive and behavioral factors that contribute to sleep disorders , The CBT-i included sleep hygiene counseling, stimulus control, cognitive restructuring, relaxation techniques, and benzodiazepine therapy or withdrawal (when needed). To conduct the intervention, guidelines for GPs and nurses and graphic and written materials for patients (sleep diary, registry of behavior habits, and cognitive problems) were developed
    Primary Outcome Measure Information:
    Title
    Acceptability of the training of PCPs
    Description
    Satisfaction with training content and its ability to provide sufficient training measured though 2 nominal groups with a previous script
    Time Frame
    3 months postintervention
    Secondary Outcome Measure Information:
    Title
    Feasibility of the intervention
    Description
    Adequacy of sessions in terms of content, duration and number, fitting in PCPs agenda and patients acceptance.
    Time Frame
    3 months postintervention
    Title
    Feasibility of the study design
    Description
    Number of patients eligible identified and included, number of PCP randomized, number of patients followed up,completion of follow up and adherence to intervention sessions.
    Time Frame
    3 months postintervention
    Title
    Intervention Effectiveness: Sleep
    Description
    The Pittsburgh Sleep Quality Index (PSQI) is a 19-items self reported questionnaire that assesses 7 clinical components of sleep quality. Each item is rated on 0 to 3 point scale in which 0 is equal to not in the past month and 3 is equal to 3 or more times a week, with a global score range from 0 to 21. A cut off score of 5 has shown to discriminate between good and bad sleepers.
    Time Frame
    pretreatment and 3 months postintervention
    Title
    Intervention Effectiveness:Anxiety
    Description
    The Hospital Anxiety and Depression Scale (HADS) measures anxiety and depression levels in the preceding week. It is 14-item self-report scale with two 7-item anxiety or depression subscales. Each item scores from 0 to 3 point scale giving maximum subscale scores of 21. Patients with scores >10 are considered to have morbidity, between 8 and 10 as borderline cases and <8 absence of relevant
    Time Frame
    pretreatment and 3 months postintervention

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: 18 to 65 years-old Diagnoses of chronic insomnia according to the Insomnia Severity Index (ISI equal or higher than 8) and had insomnia longer than 3 months; Did or did not use a hypnotic medication. Exclusion criteria: Clinical diagnosis of secondary insomnia or another sleep disorder, such as restless legs syndrome, parasomnia, or alterations of the circadian rhythm (e.g., due to shift work) Use of a medication that could produce sleep alterations Severe psychiatric disorder; depression (HADS score ≥ 8) or diagnosis of major depression in the clinical records Suicide attempt Use of an antidepressant or anti-psychotic medication Alcohol or drug abuse during the last year Reception of another CBT-i Sleep apnea Dementia or presence of a cognitive deficit (Mini Mental State Evaluation score lower than 23) Neurodegenerative or oncological disease with poor prognosis Mental or physical incapacities that impeded participation in interviews Acute or chronic pain secondary to a rheumatic disease or another untreated chronic disease Pregnancy Participation in a previous clinical trial in the participating health centers
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Isabel Torrens, MD
    Organizational Affiliation
    Santa Ponça health Care Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Data not shared
    Citations:
    PubMed Identifier
    33863276
    Citation
    Torrens I, Esteva M, Vicens C, Piza-Portell MR, Vidal-Thomas MC, Vidal-Ribas C, Lorente-Montalvo P, Torres-Solera E. Assessing the feasibility and acceptability of a cluster-randomized study of cognitive behavioral therapy for chronic insomnia in a primary care setting. BMC Fam Pract. 2021 Apr 16;22(1):77. doi: 10.1186/s12875-021-01429-5.
    Results Reference
    derived

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    Feasibility and Acceptability of Cognitive Behavioral Therapy for Chronic Insomnia in a Primary Care

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