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Improvements of physiological parameters after one single Rhythmical Massage intervention in stressed adults – a prospective, randomised, single-blinded Study

Improvements of physiological parameters after one single Rhythmical Massage intervention in stressed adults – a prospective, randomised, single-blinded Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00004164
Enrollment
123
Registered
2012-05-25
Start date
2010-01-20
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Interventions

Group 1: Participants were exposed to an experimental strained situation, the Trier Social Stress Test (TSST), before receiving a single Rhythmical massage intervention with aroma oil (lavender and tu

Sponsors

Charité - Universitätsmedizin Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: participants had to give written informed consent in participating and the transfer of their data under a pseudonym

Exclusion criteria

Exclusion criteria: acute and chronic diseases or other severe psychiatric comorbidity that could affect their participation

Design outcomes

Primary

MeasureTime frame
heart rate variability was assessed over a period of 24 hours; the assessment of the fingerbloodpressure took place prior to the massage and after over a period of 30 minutes; salivary cortisol was assessed five times prior to, during and after the massage

Secondary

MeasureTime frame
Following questionnaires were assessed prior to the massage and afterwards: existential orientation Scale from von Zerssen (Befindlichkeitsliste); list of somatic complaints from von Zerssen (Beschwerdeliste); multidimensional questionnaire on existential orientation by Steyer (Mehrdimensionaler Befindlichkeitsfragebogen); visual analog scales All questionnaires assess the actual well-being and are therefore valid assessments of short-term effects in therapy trials.

Countries

Germany

Contacts

Public ContactJenny Lena Kanitz

Charité - Universitätsmedizin Berlin

jenny-lena.kanitz@charite.de0049/ (0) 30 450 566 077

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 24, 2026