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Assessing the Impact of Clown Therapy in a Palliative Care Unit: A Prospective, Descriptive Study

Assessing the Impact of Clown Therapy in a Palliative Care Unit: A Prospective, Descriptive Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02610452
Acronym
OUPS
Enrollment
30
Registered
2015-11-20
Start date
2016-03-31
Completion date
2016-11-12
Last updated
2017-07-28

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

Conditions

Palliative Care

Keywords

clown therapy

Brief summary

The main objective of this study was to assess changes in the quality of life of patients in a Palliative Care Unit via the symptoms by the Edmonton Symptom Assessment System (ESAS) before and one hour after the passage of a clown therapist .

Detailed description

The secondary objectives of this study are to evaluate before versus after the intervention of clowns therapists: A. Changes in the quality of life at two days after the intervention (using the ESAS). B. The quality of life two days after the intervention via the McGill Quality of Life Questionnaire. C. The quality of life of patients after the intervention as assessed by semi-structured interviews conducted by the department psychologist. D. The quality of life of caregivers after the intervention as assessed by semi-structured interviews conducted by the department psychologist. E. Employee satisfaction at the end of the intervention period in the department and after debriefing as assessed by semi-structured interviews conducted by the department psychologist.

Interventions

OTHERClown therapy

The clowns intervene by twos: a game takes place. 1. The game requires the active presence of a number of potential players in the room (patient, family, caregivers) and takes into account body position, emotional state, the general atmosphere. 2. The clowns initiate a game proposal: provisional staging of clown characters based on imagination/improvisation which engages a physicality and a basic emotional state. 3. The original game proposal is adjusted according to mutual empathy with those present. 4. The game is developed on the model of theatrical improvisation: an original creation that has scenic quality comparable to that of a complete representation. Improvisation time varies depending on the condition of the person, his/her desire to participate, choosing the main theme. 5. The final stage of the game is preparing all actors for separation: restitution of roles, revisiting the paths traveled.

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* The patient must have given his/her informed and signed consent * The patient must be insured or beneficiary of a health insurance plan * Patient receiving palliative care, ie with a severe and progressive disease bringing into play vital prognosis, in advanced or terminal phase * Clinically stable patients, regardless of disease type. The existence of clinical symptoms (pain, discomfort, etc.) found at recruitment by the investigator and not affecting the mental clarity of the subject, does not justify the exclusion of the patient * Absence of cognitive disorders; since the protocol provides a clinical interview covering in particular his/her quality of life, included patients will be able to express their feelings * In addition, patients who have undergone this type of intervention (clown therapist) will not be excluded from this study.

Exclusion criteria

* The patient is participating in another study * The patient is an adult under judicial protection * The patient refuses to sign the consent * It is impossible to correctly inform the patient * Patient with an inability to fill our protocol assessment scales * Patients under treatment known to reduce the level of awareness * Patients with major cognitive impairment * Patients with symptoms that bring into question their level of awareness * Patients with significant risk factors and who should benefit from personalized monitoring from the team (clinically unstable patients, emergency situations, agitated patients, dementia, etc ...). * Patient is unable to submit to the continuity of the study.

Design outcomes

Primary

MeasureTime frameDescription
ESAS questionnaire1 hour before clown therapy sessionThe ESAS (Edmonton Symptom Assessment System) self-administered questionnaire

Secondary

MeasureTime frame
McGill Quality of Life Questionnaire1 hour before clown therapy session
Semi-directed patient interviewDay 2
Semi-directed caregiver interviewDay 0
Semi-directed staff interviewDay 0

Countries

France

Outcome results

None listed

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