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FaReWell Depression - Facial Exercise Program to Treat Depression

Facial Rehabilitation of Wellbeing in Depression: a Randomized Controled Trial of a Facial Physiotherapeutic Exercise Program in the Treatment of Depression

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03983291
Enrollment
40
Registered
2019-06-12
Start date
2019-06-01
Completion date
2025-12-01
Last updated
2024-08-07

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

Conditions

Depression

Brief summary

This study investigates if a physiotherapeutic exercise program designed to relax facial muscles associated with the expression of negative emotions and to activate and strengthen facial muscles associated with the expression of positive emotions can reduce the symptoms of depression and improve wellbeing and quality of life in the affected patients.

Detailed description

Activity of the facial musculature expresses emotions, but also generates proprioceptive signals to the emotional brain that maintain and reinforce the expressed emotions. This has been described by Charles Darwin and William James in the facial feedback hypothesis. Studies have shown that interruption of facial feedback by the injection of botulinum toxin into the corrugator and procerus muscles, which express negative emotions like sadness, anger, and fear, can reduce the symptoms of depression. In the present study we investigate, if similar effects can be achieved by a relaxing massage of these and other muscles that are associated with the expression of negative emotions and if strengthening exercises of muscles that express positive emotions, the zygomaticus and orbicularis oculi muscles, can contribute to the rehabilitation of positive emotionality in depression. After instruction by a physiotherapist, participants will practice the exercises daily for 15 minutes.

Interventions

BEHAVIORALFaReWell Depression

Facial massage and force exercise

Sponsors

Zentrum für Angst und Depressionsbehandlung Zürich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

For six weeks one arm receives the FaReWell Depression intervention and one arm receives a control resting intervention. The former arm continues on the FaReWell Depression intervention while the latter arm is switched to the FaReWell Depression intervention for another six weeks.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Mild to moderate unipolar depression * Stable treatment for at least 6 weeks

Exclusion criteria

* Organic mental disorders * Mental disorders due to psychoactive substance use * Schizophrenia and other psychotic disorders * Previous cosmetic procedures (botulinum toxin, fillers, lifting) * Facial palsy * Facial skin disorders

Design outcomes

Primary

MeasureTime frameDescription
Change in Montgomery-Asberg Depression Rating Scale (MADRS)6 weeksThe Montgomery-Asberg Depression Rating Scale (MADRS) is an expert rating scale with 10 items for the measurement of the severity of depressive symptoms. Change in depression severity is measured as change in the total score of the scale (0-60 points).

Secondary

MeasureTime frameDescription
Change in Montgomery-Asberg Depression Rating Scale (MADRS)3, 9, 12 weeksThe Montgomery-Asberg Depression Rating Scale (MADRS) is an expert rating scale with 10 items for the measurement of the severity of depressive symptoms. Change in depression severity is measured as change in the total score of the scale (0-60 points).
Change in Patient-Health-Questionnaire-9 (PHQ-9)3, 6, 9, 12 weeksThe Patient-Health-Questionnaire-9 (PHQ-9) is a self-rating scale with 9 items for the measurement of the severity of depressive symptoms. Change in depression severity is measured as change in the total score of the scale (0-27 points).
Change in Snaith-Hamilton-Pleasure-Scale (SHAPS-D)3, 6, 9, 12 weeksThe Snaith-Hamilton-Pleasure-Scale (SHAPS-D) is a self-rating scale with 14 items for the measurement of pleasure. Change in anhedonia (inability to experience pleasure) is measured as change in the total score of the scale (0-14 points).

Countries

Switzerland

Contacts

Primary ContactPatricia Waldvogel, PhD
PWaldvogel@zadz.ch+41 44 3866600
Backup ContactAxel Wollmer, MD
axel.wollmer@unibas.ch+49 151 53136738

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026