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AIR-program and HUS Internet Therapy Compared to Treatment as Usual in Functional Disorders and Post Covid-19 Condition

Primary Purpose

Functional Disorders, Post Covid-19

Status
Recruiting
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
AIR-program
HUS Internet therapy
Treatment as usual
Sponsored by
Helsinki University Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Functional Disorders

Eligibility Criteria

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

Inclusion Criteria:

  • • The criteria of bodily stress syndrome, fibromyalgia, chronic fatigue syndrome, or long Covid fulfilled AND

    • Diagnostic examinations have ruled out the potential somatic reasons for the symptoms AND
    • Disabling symptoms have lasted at least 3 months AND
    • Patient is willing to receive a psychoeducation or brain retraining intervention.

Exclusion Criteria:

  • • Patients for whom participation could be overly demanding because of physical constraints (for example, patients who cannot write because of dystonia or bedridden patients)

    • Patients with presence of severe psychiatric and severe somatic disorders, e.g. moderate or severe depression or newly onset cancer for which the study could be overly strenuous.

Sites / Locations

  • Clinic for Functional Disorders, HUSRecruiting
  • Clinic for Long Covid, HUSRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

AIR-program

HUS Internet therapy

Treatment as usual

Arm Description

• The Amygdala and insula retraining program consists of novel brain retraining approaches focused on hypothetically interrupting and retraining the conditioned defensive hyper-stimulation of the sympathetic nervous system and aspects of the immune system by the amygdala and insula, to bring the brain and body back to homeostasis. It includes supportive techniques such as breathing, meditation, and neurolinguistic programming. The patients are invited to an online program of video session and eight weekly 2 h webinar sessions followed by three monthly sessions. The patients are assigned to do daily homework that takes approximately 15 to 20 min to complete

The HUS internet therapy for bodily stress syndromes (iHUSbss) includes psychoeducation about autonomic nervous system and of the effects of patient's own thinking and action on the nervous system. The exercises aim at relaxing the body, at novel ways to observe the symptoms, and at developing acceptance and self-compassion. The program includes exercises that are done regularly in everyday life.

The patients may have appointments with their physician, physiotherapist, or another health professional, and they may attend group interventions. If possible, medication is kept the same during the intervention and three months afterwards. If there is need to change the medication during the trial, the changes will be recorded. Appointments with health professionals and attendance in group interventions are monitored.

Outcomes

Primary Outcome Measures

Change from baseline in functional ability as measured by the WHODAS2.0 instrument at six months.

Secondary Outcome Measures

Change from baseline in quality of life as measured by EUROHIS-8
Change from baseline in health related quality of life as measured by 15D
Change from baseline in symptoms as measured by SSD-12 and PHQ-15
Change from baseline in depression as measured by PHQ-9
Change from baseline in anxiety as measured by GAD-7
Change in sleep as measured by ISI
Change in resilience as measured by Resilience Scale-14

Full Information

First Posted
January 24, 2022
Last Updated
January 27, 2022
Sponsor
Helsinki University Central Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05212467
Brief Title
AIR-program and HUS Internet Therapy Compared to Treatment as Usual in Functional Disorders and Post Covid-19 Condition
Official Title
Amygdala and Insula Retraining (AIR) Program and HUS Internet Therapy Compared to Treatment as Usual in Bodily Stress Syndrome, Fibromyalgia, Post Covid-19, and Chronic Fatigue Syndrome (ME/CFS)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 31, 2022 (Anticipated)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Helsinki University Central Hospital

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 study will compare an Amygdala and insula retraining (AIR) program to an internet therapy developed at Helsinki University Hospital. The study will be a multi-center randomized controlled trial. Study units will be recruited from the Network for Functional Disorders that is hosted by the HUS Clinic for Functional Disorders and potentially later from international collaborators. The trial will clarify whether internet-based non-drug based therapies are helpful in overcoming the central sensitization and the functional disabilities caused by these disorders.
Detailed Description
Functional disorders are a challenging group of conditions treated both in primary and secondary care. Recently, mounting evidence shows that central nervous system sensitization is one of the involved mechanisms, giving new treatment opportunities. There are self-management programs and internet therapies that aim at overcoming the central sensitization by creating new neural networks in the brain. This study aims to test whether an Amygdala and insula retraining (AIR) program compared to an internet therapy developed at HUS (Helsinki University Hospital) and treatment as usual (TAU) is effective in the treatment of functional disorders, fibromyalgia, long Covid, and chronic fatigue syndrome (ME/CFS). The investigators will perform a multi-center randomized controlled trial in volunteering health units and with volunteering patients aiming at 360 patients altogether. The physicians in charge of the patients will be recruited from the Network for Functional Disorders launched by the novel clinic at HUS. The participating centers will receive an introduction in functional disorders, the underlying mechanisms, and treatment opportunities. For functional disorders, this study applies the ICD-11 primary care code of Bodily stress syndromes (BSS), which covers fibromyalgia, irritable bowel syndrome, multiple chemical sensitivities, and other, both single system and multiorgan functional disorders. In addition, for patients with fibromyalgia, chronic fatigue symptoms, and Post Covid-19 condition, we will apply specific diagnostic criteria. Both primary and secondary care treatment units that manage these disorders can recruit patients. The studied interventions are an Amygdala and insula retraining (AIR) program and an internet therapy developed at HUS, and patients receive usual care in addition to these interventions. The third study arm consists of treatment as usual for six months after which the patients receive the AIR program or the internet therapy if they so wish. When the participating physicians consider that a patient could benefit from a self-management program, they introduce the trial to the patient. The consenting patient fills in a baseline survey and is followed up at 3, 6, and 12 months with the help of the HUSeCRF (online surveys at the HUS electronic Case Report Form), or research nurse's interviews. This study will give new insight into the opportunities of self-management programs in the treatment of bodily stress syndromes, fibromyalgia, Post Covid-19, and ME/CFS. The investigators will find out whether the training programs increase patients' functional ability and quality of life as measured on a scale from 0 to 10. These scales and functional ability as measured by WHODAS 2.0 serve as main outcome measures for this study. This trial is the first large-scale randomized trial that assesses these methods developed to overcome the central sensitization of brain. The results will have an impact on the management of these common and often debilitating conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Functional Disorders, Post Covid-19

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients are randomized to one of the three treatment groups
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
360 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
AIR-program
Arm Type
Active Comparator
Arm Description
• The Amygdala and insula retraining program consists of novel brain retraining approaches focused on hypothetically interrupting and retraining the conditioned defensive hyper-stimulation of the sympathetic nervous system and aspects of the immune system by the amygdala and insula, to bring the brain and body back to homeostasis. It includes supportive techniques such as breathing, meditation, and neurolinguistic programming. The patients are invited to an online program of video session and eight weekly 2 h webinar sessions followed by three monthly sessions. The patients are assigned to do daily homework that takes approximately 15 to 20 min to complete
Arm Title
HUS Internet therapy
Arm Type
Active Comparator
Arm Description
The HUS internet therapy for bodily stress syndromes (iHUSbss) includes psychoeducation about autonomic nervous system and of the effects of patient's own thinking and action on the nervous system. The exercises aim at relaxing the body, at novel ways to observe the symptoms, and at developing acceptance and self-compassion. The program includes exercises that are done regularly in everyday life.
Arm Title
Treatment as usual
Arm Type
Placebo Comparator
Arm Description
The patients may have appointments with their physician, physiotherapist, or another health professional, and they may attend group interventions. If possible, medication is kept the same during the intervention and three months afterwards. If there is need to change the medication during the trial, the changes will be recorded. Appointments with health professionals and attendance in group interventions are monitored.
Intervention Type
Behavioral
Intervention Name(s)
AIR-program
Intervention Description
This is a guided self management program that is added on the treatment as usual.
Intervention Type
Behavioral
Intervention Name(s)
HUS Internet therapy
Intervention Description
This is a guided self management program that is added on the treatment as usual.
Intervention Type
Behavioral
Intervention Name(s)
Treatment as usual
Intervention Description
The patients receive routine care from their physician which may include drugs, visits or rehabilitation
Primary Outcome Measure Information:
Title
Change from baseline in functional ability as measured by the WHODAS2.0 instrument at six months.
Time Frame
3, 6 and 12 months
Secondary Outcome Measure Information:
Title
Change from baseline in quality of life as measured by EUROHIS-8
Time Frame
3, 6 and 12 months
Title
Change from baseline in health related quality of life as measured by 15D
Time Frame
3, 6 and 12 months
Title
Change from baseline in symptoms as measured by SSD-12 and PHQ-15
Time Frame
3, 6 and 12 months
Title
Change from baseline in depression as measured by PHQ-9
Time Frame
3, 6 and 12 months
Title
Change from baseline in anxiety as measured by GAD-7
Time Frame
3, 6 and 12 months
Title
Change in sleep as measured by ISI
Time Frame
3, 6 and 12 months
Title
Change in resilience as measured by Resilience Scale-14
Time Frame
3, 6 and 12 months

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: • The criteria of bodily stress syndrome, fibromyalgia, chronic fatigue syndrome, or long Covid fulfilled AND Diagnostic examinations have ruled out the potential somatic reasons for the symptoms AND Disabling symptoms have lasted at least 3 months AND Patient is willing to receive a psychoeducation or brain retraining intervention. Exclusion Criteria: • Patients for whom participation could be overly demanding because of physical constraints (for example, patients who cannot write because of dystonia or bedridden patients) Patients with presence of severe psychiatric and severe somatic disorders, e.g. moderate or severe depression or newly onset cancer for which the study could be overly strenuous.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Helena Liira, MD, PhD
Phone
+358 50 577 1351
Email
helena.liira@hus.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Jari Arokoski, Prof
Phone
+358 50 428 7901
Email
jari.arokoski@hus.fi
Facility Information:
Facility Name
Clinic for Functional Disorders, HUS
City
Helsinki
ZIP/Postal Code
00029
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Markku Sainio, MD, PhD
Phone
+358 40 569 3186
Email
markku.sainio@hus.fi
Facility Name
Clinic for Long Covid, HUS
City
Helsinki
ZIP/Postal Code
00029
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Helena Liira, MD, PhD
Phone
+358 50 577 1351
Email
helena.liira@hus.fi

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
We have applied for EU Horizon funding and may share data in that project.

Learn more about this trial

AIR-program and HUS Internet Therapy Compared to Treatment as Usual in Functional Disorders and Post Covid-19 Condition

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