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Evaluation of Spa Treatment on Insomnia (SOMNOTHERM)

Primary Purpose

Insomnia

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Computerized behavioral therapy program delivered by internet for insomnia management
Spa treatment
Sponsored by
Association Francaise pour la Recherche Thermale
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring Spa treatment, Cognitive Behavioral Therapy, Internet delivered self-help program, Insomnia, Sleep restriction, stimulus control, crenotherapy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female aged between 18 and 80 years old
  • Registered at one of the participating spas, for a psychosomatic spa treatment scheduled for the next 12 months, but within a period of more than 16 weeks.
  • ISI score ≥ 8 on the pre-selection questionnaire
  • Person with a persistent insomnia disorder, with or without comorbidities, according to DSM 5
  • Owning or having access to a computer / tablet or smartphone and to an internet connection
  • Affiliated to a national health service
  • Having given written informed consent to participate in the trial.

Exclusion Criteria:

  • Strong suspicion of obstructive sleep apnea (OSA) syndrome on the STOP-BANG questionnaire and restless legs syndrome on the RLS screening questionnaire
  • Having started antidepressant treatment in the last 2 months or whose treatment dose has been increased in the last 2 months
  • Having started treatment with anxiolytic, hypnotic or neuroleptic in the last month or whose dosage of treatment has been increased in the last month
  • Having carried out a spa treatment in the last 6 months, whatever the specialty.
  • Registered to follow a complementary program for insomnia disorders during the planned spa treatment
  • Pregnant or lactating women
  • Major under guardianship or curatorship
  • Night and shift-workers
  • Having undertaken trans-meridian travel (± 3H) in the previous 1 month

Sites / Locations

  • University Hospital, BordeauxRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Internet Behavioral therapy program + spa therapy

Internet Behavioral therapy program at home

Arm Description

Patient following a program of computerized behavioral therapy for insomnia management during a 3 weeks spa treatment.

Patient following a program of computerized behavioral therapy for insomnia management during 3 weeks at home.

Outcomes

Primary Outcome Measures

Insomnia Severity Scale (ISI) score
7-item questionnaire assessing insomnia nature, severity and impact. The global score ranges from 0 to 28.

Secondary Outcome Measures

Total sleep time (TST) obtained by sleep diary
Total sleep time = total sleep episode minus awake time. Subject records in his online sleep diary bedtime, wake-up time, time asleep, intra-night awakenings.
Sleep efficiency (SE) obtained by sleep diary
Ratio of total sleep time (TST) to time in bed (TIB) (multiplied by 100 to yield a percentage). Subject records in his online sleep diary bedtime, wake-up time, time asleep, intra-night awakenings.
Sleep latency obtained by sleep diary
Length of time to accomplish the transition from full wakefulness to sleep. Subject records in his online sleep diary bedtime, wake-up time, time asleep, intra-night awakenings.
Insomnia Severity Scale (ISI) score
7-item questionnaire that assesses insomnia nature, severity and impact.
EQ-5-D
Standardized instrument for measuring generic health status.
The Presleep State Arousal Scale (PSAS)
16-item questionnaire assessing whether the respondent experienced somatic (8 items, eg heart rate) or cognitive hyperarousal (eg racing thoughts) at bedtime
Hospital Anxiety and Depression Scale (HAD)
14-item scale that generates ordinal data. Seven of the items relate to anxiety and seven relate to depression.
Short Version of the Functional Outcomes of Sleep Questionnaire (FOSQ)
10 item questionnaire assessing the impact of excessive sleepiness on activities of daily living
Rate of discontinuation and rate of reduction of anxiolytic hypnotic drugs and hypnotics
Every day anxiolytic hypnotic drugs and hypnotics daily dose
Acceptability E-scale (AES)
6-item self-reported questionnaire that evaluates the extent to which patients find E-health systems acceptable
Client Satisfaction Questionnaire (CSQ-8)
8-item questionnaire easily scored and administered measurement that is designed to measure client satisfaction with services.
Sleep Condition Indicator (SCI)
brief 8-item scale which measures sleep problems against the DSM-5 criteria for insomnia disorder
The Pittsburgh Sleep Quality Index (PSQI)
self-report questionnaire that assesses sleep quality over a 1-month time interval
Cognitive Scale of Attachment to Benzodiazepines ("Echelle cognitive d'attachement aux benzodiazépines" ECAB)
10-item scale assessing cognitive component of attachment to benzodiazepines
The Munich ChronoType Questionnaire (MCTQ)
Questionnaire to determine Chrono Type.
The Epworth Sleepiness Scale (ESS)
8-item questionnaire assessing daytime sleepiness
Freiburg Mindfulness Inventory - short version (FMI)
questionnaire for measuring mindfulness
Krueger's personality inventory for DSM-5 in its brief form (PID-5-BF)
25-item self-report questionnaire assessing the presence and severity of the five maladaptive personality traits outlined in DSM-5.
The Arousal Predisposition Scale (APS)
12-item questionnaire assessing whether the respondent considers her/himself a stressful and emotionally reactive person
The Ford Insomnia to Stress Scale (FIRST)
9-item questionnaire assessing whether past and future stressful events are likely to affect sleep quality
The "locus of control for technology"-questionnaire ("Kontrollüberzeugungen im Umgang mit Technik" - KUT)
8-item questionnaire assessing the specific interaction with technical environments of users

Full Information

First Posted
June 17, 2019
Last Updated
May 25, 2022
Sponsor
Association Francaise pour la Recherche Thermale
Collaborators
University Hospital, Bordeaux, University of Bordeaux
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1. Study Identification

Unique Protocol Identification Number
NCT03991247
Brief Title
Evaluation of Spa Treatment on Insomnia
Acronym
SOMNOTHERM
Official Title
Evaluation of Psychosomatic Spa Treatment With Crenotherapy to Potentiate the Implementation of Behavioral Measures for Insomnia Disorder Management
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 5, 2019 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Association Francaise pour la Recherche Thermale
Collaborators
University Hospital, Bordeaux, University of Bordeaux

4. Oversight

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

5. Study Description

Brief Summary
Persistant insomnia is a common sleep disorder that affects approximately 20% of the French population. The standard treatment for chronic insomnia is Cognitive-Behavioral Therapy (CBT). Behavioral measures can be difficult to implement for the patient alone at home. Spa therapy with psychosomatic orientation allows to implement hygiene rules and structure rhythms of life. In addition, recent studies have shown that spa treatment, including crenotherapy, is effective in somatic complaints related to anxiety and benzodiazepine withdrawal. The spa treatment could therefore provide ideal conditions for the implementation of behavioral measures for insomnia management. The objective of SOMNOTHERM study is to measure efficiency on insomnia complaints at 8 weeks of a the implementation of a Behavioral therapy program for insomnia delivered by an internet software combined to a spa treatment compared to implementation of the same program at home (standard care).
Detailed Description
Persistant insomnia is a common sleep disorder that affects approximately 20% of the French population. The standard treatment for chronic insomnia is Cognitive-Behavioral Therapy (CBT). This therapy is based on 4 components: sleep restriction, stimulus control, cognitive therapy and sleep hygiene education. Unfortunately, there are an insufficient number of trained CBT experts especially in France. Online programs based on CBT principles (e-CBT) have been proved to be effective in improving the sleep and daytime functioning in this population. Thus e-CBT can be an effective alternative to conventional CBT. Behavioral measures, however, remains difficult for patients to implement alone at home. Spa therapy with psychosomatic orientation allows to implement hygiene rules and structure rhythms of life. In addition, recent studies have shown that spa treatment, including crenotherapy, is effective in somatic complaints related to anxiety and benzodiazepine withdrawal. In this context, spa treatment with psychosomatic orientation appears conducive to implement hygiene rules and structure rhythms of life. The spa treatment could therefore provide ideal conditions for the implementation of behavioral measures of insomnia management (sleep hygiene, stimulus control and time in bed restriction) and could have a very beneficial effect on persistent insomnia disorder. This non-pharmacological therapy could also reduce hypnotics consumption (especially benzodiazepine). The main hypothesis of the study is that behavioral measures of insomnia management delivered by an internet software program combined to a spa treatment will be more effective on insomnia complaints (evaluated at 8 weeks) than the same program implemented at home. Patients will be followed during 6 months after the beginning of the program. Subjects' recruitment will be carried out from the list of patients registered for a spa treatment in one of the five spa centers participating in the study (Les Thermes de Saujon, Les Grands Thermes de Bagnères de Bigorre, Les Thermes de Divonne-les-Bains, Les thermes de Néris-les-Bains, Les Thermes d'Ussat-les-Bains). Study visits will be conducted by the coordinating center (CHU Bordeaux) by telephone interviews or video calls with participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia
Keywords
Spa treatment, Cognitive Behavioral Therapy, Internet delivered self-help program, Insomnia, Sleep restriction, stimulus control, crenotherapy

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Internet Behavioral therapy program + spa therapy
Arm Type
Experimental
Arm Description
Patient following a program of computerized behavioral therapy for insomnia management during a 3 weeks spa treatment.
Arm Title
Internet Behavioral therapy program at home
Arm Type
Active Comparator
Arm Description
Patient following a program of computerized behavioral therapy for insomnia management during 3 weeks at home.
Intervention Type
Behavioral
Intervention Name(s)
Computerized behavioral therapy program delivered by internet for insomnia management
Intervention Description
The online program consists in restriction of time in bed and stimulus control instructions. First, patient will complete an on-line sleep diary during 2 weeks. The personalized program is then activated by a practitioner (phone interview) who both assesses restriction of time in bed and delivers instructions of stimulus control. Then, restriction of time in bed is administered by the internet-delivered self-help program. The participant still completes his on-line sleep diary every day. Every 7 days, according mean sleep efficiency, a new sleep schedule recommendation is given to the participant. In addition, the program delivers everyday a set of instructions (stimulus control) designed to re-associate the bed/bedroom with sleep and to re-establish a consistent sleep wake schedule. The duration of restriction of time in bed program is 3 weeks (during spa treatment or at home depending on the allocated arm).
Intervention Type
Other
Intervention Name(s)
Spa treatment
Intervention Description
Spa treatment is harmonized in the different stations. It consists in: a medical thermal follow-up: weekly medical consultation of 15 minutes during the 3 weeks spa treatment. an institutional follow-up: support, help and monitoring of patients during spa treatment Crenotherapy: 18 baths of 10 minutes in running water, 18 spa showers of 3 minutes, 9 massages under water of 20 minutes, 18 baths of 10 minutes in pool. Water temperature of pool is between 31°C and 33°C. Water temperature for other care is 35°C and 38°C.
Primary Outcome Measure Information:
Title
Insomnia Severity Scale (ISI) score
Description
7-item questionnaire assessing insomnia nature, severity and impact. The global score ranges from 0 to 28.
Time Frame
Week 10 = 8 weeks after beginning of computerized behavioral therapy (starting of time in bed restriction)
Secondary Outcome Measure Information:
Title
Total sleep time (TST) obtained by sleep diary
Description
Total sleep time = total sleep episode minus awake time. Subject records in his online sleep diary bedtime, wake-up time, time asleep, intra-night awakenings.
Time Frame
Every night between starting of sleep diary completion (Day 0) and Month 6 (study termination)
Title
Sleep efficiency (SE) obtained by sleep diary
Description
Ratio of total sleep time (TST) to time in bed (TIB) (multiplied by 100 to yield a percentage). Subject records in his online sleep diary bedtime, wake-up time, time asleep, intra-night awakenings.
Time Frame
Every night between starting of sleep diary completion (Day 0) and Month 6 (study termination)
Title
Sleep latency obtained by sleep diary
Description
Length of time to accomplish the transition from full wakefulness to sleep. Subject records in his online sleep diary bedtime, wake-up time, time asleep, intra-night awakenings.
Time Frame
Every night between starting of sleep diary completion (Day 0) and Month 6 (study termination)
Title
Insomnia Severity Scale (ISI) score
Description
7-item questionnaire that assesses insomnia nature, severity and impact.
Time Frame
On Day 0, Week 5, Week 7, Month 4, Month 6
Title
EQ-5-D
Description
Standardized instrument for measuring generic health status.
Time Frame
On Day 0, Week 5, Week 7, Week 10, Month 4, Month 6
Title
The Presleep State Arousal Scale (PSAS)
Description
16-item questionnaire assessing whether the respondent experienced somatic (8 items, eg heart rate) or cognitive hyperarousal (eg racing thoughts) at bedtime
Time Frame
On Day 0, Week 5, Week 7, Week 10, Month 4, Month 6
Title
Hospital Anxiety and Depression Scale (HAD)
Description
14-item scale that generates ordinal data. Seven of the items relate to anxiety and seven relate to depression.
Time Frame
On Day 0, Week 5, Week 7, Week 10, Month 4, Month 6
Title
Short Version of the Functional Outcomes of Sleep Questionnaire (FOSQ)
Description
10 item questionnaire assessing the impact of excessive sleepiness on activities of daily living
Time Frame
On Day 0, Week 5, Week 7, Week 10, Month 4, Month 6
Title
Rate of discontinuation and rate of reduction of anxiolytic hypnotic drugs and hypnotics
Description
Every day anxiolytic hypnotic drugs and hypnotics daily dose
Time Frame
On Day 0, Week 5, Week 7, Week 10, Month 4, Month 6
Title
Acceptability E-scale (AES)
Description
6-item self-reported questionnaire that evaluates the extent to which patients find E-health systems acceptable
Time Frame
On week 10 (after computerized behavioral therapy program)
Title
Client Satisfaction Questionnaire (CSQ-8)
Description
8-item questionnaire easily scored and administered measurement that is designed to measure client satisfaction with services.
Time Frame
On week 10 (after computerized behavioral therapy program)
Title
Sleep Condition Indicator (SCI)
Description
brief 8-item scale which measures sleep problems against the DSM-5 criteria for insomnia disorder
Time Frame
On Day 0
Title
The Pittsburgh Sleep Quality Index (PSQI)
Description
self-report questionnaire that assesses sleep quality over a 1-month time interval
Time Frame
On Day 0
Title
Cognitive Scale of Attachment to Benzodiazepines ("Echelle cognitive d'attachement aux benzodiazépines" ECAB)
Description
10-item scale assessing cognitive component of attachment to benzodiazepines
Time Frame
On Day 0
Title
The Munich ChronoType Questionnaire (MCTQ)
Description
Questionnaire to determine Chrono Type.
Time Frame
On Day 0
Title
The Epworth Sleepiness Scale (ESS)
Description
8-item questionnaire assessing daytime sleepiness
Time Frame
On Day 0
Title
Freiburg Mindfulness Inventory - short version (FMI)
Description
questionnaire for measuring mindfulness
Time Frame
On Day 0
Title
Krueger's personality inventory for DSM-5 in its brief form (PID-5-BF)
Description
25-item self-report questionnaire assessing the presence and severity of the five maladaptive personality traits outlined in DSM-5.
Time Frame
On Day 0
Title
The Arousal Predisposition Scale (APS)
Description
12-item questionnaire assessing whether the respondent considers her/himself a stressful and emotionally reactive person
Time Frame
On Day 0
Title
The Ford Insomnia to Stress Scale (FIRST)
Description
9-item questionnaire assessing whether past and future stressful events are likely to affect sleep quality
Time Frame
On Day 0
Title
The "locus of control for technology"-questionnaire ("Kontrollüberzeugungen im Umgang mit Technik" - KUT)
Description
8-item questionnaire assessing the specific interaction with technical environments of users
Time Frame
On Day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female aged between 18 and 80 years old Registered at one of the participating spas, for a psychosomatic spa treatment scheduled for the next 12 months, but within a period of more than 16 weeks. ISI score ≥ 8 on the pre-selection questionnaire Person with a persistent insomnia disorder, with or without comorbidities, according to DSM 5 Owning or having access to a computer / tablet or smartphone and to an internet connection Affiliated to a national health service Having given written informed consent to participate in the trial. Exclusion Criteria: Strong suspicion of obstructive sleep apnea (OSA) syndrome on the STOP-BANG questionnaire and restless legs syndrome on the RLS screening questionnaire Having started antidepressant treatment in the last 2 months or whose treatment dose has been increased in the last 2 months Having started treatment with anxiolytic, hypnotic or neuroleptic in the last month or whose dosage of treatment has been increased in the last month Having carried out a spa treatment in the last 6 months, whatever the specialty. Registered to follow a complementary program for insomnia disorders during the planned spa treatment Pregnant or lactating women Major under guardianship or curatorship Night and shift-workers Having undertaken trans-meridian travel (± 3H) in the previous 1 month
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Arthur MICOULAUD-FRANCHI, MDPhD
Phone
557820173
Ext
+33
Email
jean-arthur.micoulaud-franchi@chu-bordeaux.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Cécile KLOCHENDLER
Phone
557821159
Ext
+33
Email
cecile.klochendler@chu-bordeaux.fr
Facility Information:
Facility Name
University Hospital, Bordeaux
City
Bordeaux
ZIP/Postal Code
33000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Arthur MICOULAUD-FRANCHI, MDPhD
Phone
557820173
Ext
+33
Email
jean-arthur.micoulaud-franchi@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Cécile KLOCHENDLER
Phone
557821159
Ext
+33
Email
cecile.klochendler@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Jean-Arthur MICOULAUD-FRANCHI, MDPhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Patient could request investigator or Data Protection Officer an access to IPD according to French regulation (act No. 78-17 of 6 January 1978 on data processing, data files and individual liberties, amended by act No. 2004-801 of 6 August 2004) and he EU General Data Protection Regulation (GDPR) of 27 april 2016 applicable since 25 May 2018.

Learn more about this trial

Evaluation of Spa Treatment on Insomnia

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