Auditory Beat Stimulation and Behavioural Variant of Frontotemporal Dementia

Sponsor
University Hospital, Bonn (Other)
Overall Status
Completed
CT.gov ID
NCT05917886
Collaborator
(none)
11
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2
8
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Study Details

Study Description

Brief Summary

The goal of this study is to examine the effects of auditory beat stimulation on anxiety in patients diagnosed with bvFTD. Main aims are:

  • to ascertain whether anxiety in bvFTD patients can be modulated using auditory beat stimulation

  • to investigate patterns of anxiety and mind wandering in bvFTD patient population

Patients were asked to complete a number of questionnaires relating to well-being and mind wandering, as well as to listen daily to audio files of beat stimulation.

Condition or Disease Intervention/Treatment Phase
  • Other: Auditory beat stimulation: 8Hz monaural beat stimulation
N/A

Detailed Description

Eligible patients and their caregivers were asked to give informed written consent, if they wished to participate after an initial interview. Once enrolled, they began the study by joining a consultation with their consultant neurologist and the study coordinator. Patients each received a handbook to guide them day by day during the course of the study and an mp3 player containing the auditory beat stimulation files. The handbook also contained copies of the questionnaires the patients were asked to complete at different points during the two week study (mind wandering questionnaire, State-Trait Anxiety Inventory, Beck Depression Inventory, Rogers' Happy/ Sad Face Scale). Over the course of two weeks patients completed the questionnaires and listened daily to an auditory beat stimulation or a control recording for 20 mins at home.

Study Design

Study Type:
Interventional
Actual Enrollment :
11 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Patients participated in both the control and active auditory beat conditions, each lasting 1 week. Conditions were randomised across participants.Patients participated in both the control and active auditory beat conditions, each lasting 1 week. Conditions were randomised across participants.
Masking:
Double (Participant, Care Provider)
Masking Description:
Participants were unaware which auditory beat stimulation condition they received in which order.
Primary Purpose:
Basic Science
Official Title:
Auditory Beat Stimulation and Behavioural Variant of Frontotemporal Dementia
Actual Study Start Date :
Jan 1, 2021
Actual Primary Completion Date :
Aug 1, 2021
Actual Study Completion Date :
Sep 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Monaural beat stimulation

20 min sound recording of 8Hz monaural beat

Other: Auditory beat stimulation: 8Hz monaural beat stimulation
Auditory beat stimulation is a reversible, non-invasive application of sound to the ears.

Sham Comparator: Control

20 min sound recording of 220Hz pure sine wave

Other: Auditory beat stimulation: 8Hz monaural beat stimulation
Auditory beat stimulation is a reversible, non-invasive application of sound to the ears.

Outcome Measures

Primary Outcome Measures

  1. Examine anxiety modulation effects of monaural beat stimulation using the State-Trait Anxiety Inventory (STAI-S and T) [3 years]

    The STAI Inventory was used to assess the patients' state (STAI-S) and trait (STAI-T) anxiety. The two subscores differentiate between transient feelings of anxiety (state anxiety), i.e. those related to a particular context like an event, and anxiety levels that are more of a personal characteristic of an individual (trait anxiety: Spielberger et al., 1983). Patients responded to 20 statements contained in each subscore, using a 4-point Likert scale (not at all: 1; a little: 2; quite: 3; very: 4). The STAI Inventory was completed at the beginning and end of each week.

  2. Examine depression modulation effects of monaural beat stimulation using the Beck Depression Inventory [3 years]

    metric used to assess levels of depression; The BDI is a 21-item multiple-choice questionnaire (Beck et al., 1996). The BDI was used to assess symptoms of depression, and was administered at the beginning and end of each week, prior to the six-day daily course of auditory beat stimulation. The BDI is categorised into the following scoring ranges: 0-13 minimal; 14-19 mild; 20-28 moderate and 29-63 severe.

  3. Examine mind wandering modulation effects of monaural beat stimulation using the Mind Wandering Questionnaire [3 years]

    The Mind Wandering Questionnaire is a short-form scale intended to measure the propensity to mind wander (Mrazek et al., 2013). The questionnaire consists of five items that evaluate trait levels of mind wandering. Trait mind wandering is scored across a 6-point Likert scale (1: almost never; 2: very infrequently; 3: somewhat infrequently; 4: somewhat frequently; 5: very frequently; 6: almost always). Patients completed this questionnaire, also at the beginning and end of each week.

  4. Examine daily momentary subjective levels of anxiety, mood and pain modulation effects of monaural beat stimulation using the Mind Wandering Questionnaire [3 years]

    The Rogers' Happy/ Sad Face Scale is a visual-numeric scale that was intended to capture the momentary subjective levels of anxiety, mood and pain. Patients had to grade their feelings according to a corresponding face icon which represented a 'happy face' at the most positive end (value of 0) of the graded scale, all the way to a 'crying face' icon at the most negative end of the scale (value of 4). Patients completed this scale twice daily, once immediately prior to the auditory stimulation, and then immediately after the stimulation had concluded.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Inclusion criteria are the international criteria of a behavioral variant of FTD according to Raskovsky and colleagues (2011), which include:
  1. Early disinhibition B. Early apathy or passivity C. Early loss of compassion or empathy
  2. speech or motor stereotypies E. Hyperorality and altered eating habits F. Neuropsychological profile with executive function deficits with relatively unchanged memory and visuospatial performance G. Disruption of daily living skills H. Matching imaging (cMRI, cCT, PET).
Exclusion Criteria:
  • Exclusion criteria include the presence of a non-neurodegenerative psychiatric disease that can better explain the behavioral abnormalities or evidence of biomarkers with clear evidence of Alzheimer's disease or other neurodegenerative process

Contacts and Locations

Locations

Site City State Country Postal Code
1 Juergen Fell Bonn NRW Germany 53127

Sponsors and Collaborators

  • University Hospital, Bonn

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Juergen Fell, Priniciple Investigator, University Hospital, Bonn
ClinicalTrials.gov Identifier:
NCT05917886
Other Study ID Numbers:
  • 308/20
First Posted:
Jun 26, 2023
Last Update Posted:
Jun 26, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 26, 2023