Complex Regional Pain Syndrome Clinical Trials

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Effect of Dance-therapy on Chronic Adolescent Pain Patients - a Randomized Controlled Trial Study

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Pain, when it becomes chronic, can be a threat to patients and it is very common to observe a fear of pain and a fear of movement (kinesiophobia). Avoidance of movement due to fear of pain can lead to a deterioration of body image. Non-medicinal therapies are essential to correct this fear and movement avoidance behavior, to decrease catastrophic judgments and thus anxiety. The use of art-therapy in the accompaniment of patients with pain has shown, in particular, decreases in the intensity of pain, the level of anxiety, an improvement in stress, mood and overall psychological state. However, according to the current literature, it appears that 1) this technique is rarely used in children or adolescents, for whom non-medicinal therapies are fundamental, and 2) in the case of chronic pain, the form of art used is very rarely related to the body (most often painting, drawing, music...). In this project, investigators propose to set up and test the potential benefit of art-therapy sessions related to the body, namely dance-therapy, in adolescents and young adults suffering from chronic pain.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 20
Healthy Volunteers: f
View:

• Patients aged 12 to 20 years, girls or boys, with chronic pain.

• Diagnosis of chronic pain made in a Pain Management Center

• Patients followed in a Pain Management Center (to ensure that patients entering the protocol have pain that is not relieved by conventional treatments)

• Patients who have given written consent for adults or whose parents have given consent for minors

• Patients who are affiliated with or benefit from a social security system.

Locations
Other Locations
France
Neuroscience Research Center of Lyon (CRNL)- INSERM U1028 - NEUROPAIN laboratory
RECRUITING
Bron
Contact Information
Primary
Maud FROT, INSERM Researcher
maud.frot@univ-lyon1.fr
04 72 35 78 88
Backup
Caroline PERCHET, research engineer
caroline.perchet@univ-lyon1.fr
04 72 35 78 88
Time Frame
Start Date: 2024-03-01
Estimated Completion Date: 2030-10
Participants
Target number of participants: 160
Treatments
No_intervention: Control group
Patients in the control group will not participate in any art-therapy or yoga interventions. They will be asked to complete pain and sleep diaries, questionnaires and pain, fatigue and mood scales at the same times and for the same duration as the other groups.
Experimental: Dance-therapy group
Patients in the dance-therapy group will attend a weekly session of dance-therapy between weeks 1 and 15 of the protocol (15 sessions). They will be asked to complete daily pain and sleep diaries at weeks W0, W5, W16, W20 and W28 as well as questionnaires (kinesiophobia, anxiety, catastrophizing, fear of pain, quality of life, body image/self-perception). They will also be asked to assess their pain, fatigue and mood levels at the end of each week between W1 and W15.
Experimental: Art-therapy group
Patients in the art-therapy group will attend a weekly session of art-therapy (drawings, collages…) between weeks 1 and 15 of the protocol (15 sessions). They will be asked to complete daily pain and sleep diaries at weeks W0, W5, W16, W20 and W28 as well as questionnaires (kinesiophobia, anxiety, catastrophizing, fear of pain, quality of life, body image/self-perception). They will also be asked to assess their pain, fatigue and mood levels at the end of each week between W1 and W15.
Experimental: Yoga group
Patients in the yoga group will attend a weekly session of Vinyasa yoga between weeks 1 and 15 of the protocol (15 sessions). They will be asked to complete daily pain and sleep diaries at weeks W0, W5, W16, W20 and W28 as well as questionnaires (kinesiophobia, anxiety, catastrophizing, fear of pain, quality of life, body image/self-perception). They will also be asked to assess their pain, fatigue and mood levels at the end of each week between W1 and W15.
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov