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Group Hypnosis for Stress Reduction (Hypnostress)

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Completed

Conditions

Stress, Psychological

Treatments

Behavioral: Group hypnosis

Study type

Interventional

Funder types

Other

Identifiers

NCT03402074
Hypnostress

Details and patient eligibility

About

This prospective feasibility study aims to test a 5 week group hypnosis training as intervention to reduce perceived psychological stress in healthy subjects.

Full description

In a pre- post comparison the feasibility of a standardized weekly 90 minutes group hypnosis training including CDs/MP3 recordings as homework to reduce perceived psychological stress in healthy subjects is investigated. Outcomes are measured quantitatively and qualitatively.

Enrollment

15 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy or health-stable participants between 18 and 70 years with subjective increased intensity of stress in the last four weeks on the visual analogue scale rated between 40 -100 mm (VAS 0 - 100 mm)
  • Ability to consent and sign declaration of informed consent

Exclusion criteria

  • Current or planned participation in a stress management program within the next 17 weeks
  • Current use of psychotherapeutic treatment
  • presence of moderate or severe acute or chronic disease
  • presence of an acute or chronic mental disorder
  • Participation in a study within the last 2 months prior to enrollment
  • Lack of understanding of the German language

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Group Hypnosis
Experimental group
Description:
5 sessions of group hypnosis, each 90 minutes; plus CDs/MP3 recordings to train at home
Treatment:
Behavioral: Group hypnosis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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