CClinicalTrials.gg
Status unknownNCT04290117Updated Feb 28, 2020

Chronobiological and ACT-based Training to Handle Stress at Work

An interventional study of Acceptance and Commitment Training and Sleep Hygiene and bright light in the morning in Stress, sponsored by Psychiatric Hospital of the University of Basel. Status unknown at 1 site in Switzerland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-02-28.

Sponsored by Psychiatric Hospital of the University of Basel · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2020), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim of the present project is to combine "Acceptance and Commitment Therapy" and "sleep hygiene + light-therapy (so-called chronotherapy)" serially in a sample of employees to reduce levels of subjective exhaustion.

02

Conditions studied

  • Stress

Keywords

  • Sleep Hygiene
  • Morning Light
  • Acceptance and Commitment Training
03

In context

Lead sponsor

Psychiatric Hospital of the University of Basel is the lead sponsor of 8 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • working in an office mainly (i.e., > 60% of work time)
  • Age: ≥18 years old
  • Sex: male and female individuals
  • Ownership of cell phone with internet connection
  • informed consent as documented by signature

Exclusion criteria

Exclusion Criteria:

  • diseases of the retina or related diseases such as diabetes mellitus
  • taking drugs which heighten photosensitivity
  • inability to understand and follow procedures in German
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    ACT-Chrono

    First Acceptance and Commitment (ACT) training, followed by chronobiological training

    Behavioral: Acceptance and Commitment Training · Behavioral: Sleep Hygiene and bright light in the morning

  • Experimental
    Chrono-ACT

    First chronobiological training, followed by ACT training

    Behavioral: Acceptance and Commitment Training · Behavioral: Sleep Hygiene and bright light in the morning

  • Other
    Chrono

    First no training, followed by chronobiological training

    Behavioral: Sleep Hygiene and bright light in the morning

  • Other
    ACT

    First no training, followed by ACT training

    Behavioral: Acceptance and Commitment Training

Interventions

  • BehavioralAcceptance and Commitment Training

    During the ACT-based intervention, participants will get 4 training sessions in groups, once a week for an hour. Additionally, participants will be asked to implement behavioural exercises such as mindfulness and value-based exercises into their daily schedule.

  • BehavioralSleep Hygiene and bright light in the morning

    During the chronobiological intervention, participants will get 4 training sessions in groups, one hour per week. Additionally, they will use a daylight lamp at home, for 30 minutes per day after waking up.

06

What researchers measure

Primary outcomes

  1. Change in subjective exhaustion measured by the German Version of the Shirom-Melamed Burnout Measure

    Overall mean score as well as three subscales of Shirom-Melamed Burnout Measure ( P = physical fatigue; E= emotional exhaustion; and C= cognitive weariness, each ranging from 1-7). Note: Higher scores indicate higher levels of exhaustion (overall as well as on each scale P, E and C)

    Time frame: approx. every two weeks, and at follow up (i.e., approx. 5 weeks after last training session)

Secondary outcomes

  1. Change in Subjective well-being as assessed by General Health Questionnaire (GHQ-12)

    Sum over twelve items, higher scores indicate worse psychological well-being

    Time frame: approx. every two weeks, and at follow up (i.e., approx. 5 weeks after last training session)

  2. Change in subjective well-being as assessed by the Patient Health Questionnaire (PHQ-D)

    Sum over each of the subscales assessing somatic, depressive, anxiety and stress symptoms. The subscale assessing panic symptoms, alcohol abuse and intake of medication will be categorically evaluated.

    Time frame: approx. every 4 weeks

  3. Change in quality of circadian rhythm

    Actimetric devices are worn during 2 x 28 days continuously. These devices store the amount of activity in a resolution of 30 Hz 24/7. For data analyses, these activity data will be aggregated to three values (stability, variability and relative amplitude) per participant and training episode by non-parametric circadian rhythm analyses; higher values indicate higher stability, variability and amplitude

    Time frame: Actimetric devices are worn during 2 x 28 days continuously. The outcome of actimetric data are aggregated per person and training episode

  4. Change in subjective and objective sleep quality: Pittsburgh Sleep Quality Index (PSQI)

    Subjectively assessed by the Pittsburgh Sleep Quality Index (PSQI, higher scores indicate worse subjective sleep quality), by a single question about sleep quality (higher scores indicate worse quality) and by actimetric analyses

    Time frame: PSQI is collected approx. every four weeks and at follow up (i.e. approx 5 weeks after last training), the single question and actimetric data are measured daily

  5. Change in Subjective sleepiness in the morning

    Measured by Karolinska Sleepiness Scale (KSS), higher scores indicate higher sleepiness

    Time frame: KSS is measured daily

  6. Change in daytime subjective sleepiness

    Measured by Epworth Sleepiness Scale (ESS): higher scores indicate higher sleepiness

    Time frame: ESS approx every four weeks

  7. Change in Chronotype

    Measured by a short version of the Munich Chronotype Questionnaire, higher scores indicate a later chronotype

    Time frame: approx. every 4 weeks and at follow up (i.e., approx. 5 weeks after last training session)

  8. Change in Burnout severity

    Measured by Maslach Burnout Inventory using sumscores of the subscales emotional exhaustion, depersonalization and personal achievement. Higher scores indicate higher exhaustion, depersonalization and better personal achievement

    Time frame: every 4 weeks

  9. Change in Absences

    Numbers of days absent if available from the employer

    Time frame: Assessed daily

  10. Change in Implementation of treatment

    Questions about frequency implementation of treatment in daily life

    Time frame: approx. every two weeks, and at follow up (i.e., approx. 5 weeks after last training session)

07

Study locations

1 of 1 sites recruiting
  • Centre for Chronobiology, UPK Basel
    Basel, 4002, Switzerland
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 28, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04290117
Lead sponsor
Psychiatric Hospital of the University of Basel
Responsible party
Carolin Reichert (Principal Investigator, Psychiatric Hospital of the University of Basel) — Principal investigator
First posted
Feb 28, 2020
Start date
Oct 16, 2019
Primary completion
Mar 2020 (estimated)
Completion
Apr 2020 (estimated)
Last update
Feb 28, 2020

Study contacts

Carolin Reichert, PhD
Contact
carolin.reichert@upk.ch
+41 61 325 5508
Carolin Reichert, PhD
principal investigator · Centre for Chronobiology

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

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