Feasability and Clinical Impact Study of Non Pharmacological Interventions in Management of Chronic Pain
CompletedNot applicableNCT04176341
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
This feasability study aims to compare the 6-month success rate of a systematic proposal for non pharmacological interventions targeting the subject's empowerment among slackline, mindfulness, adapted physical activity, self-hypnosis, and Qi Gong versus usual care in the management of chronic pain.
Study details
- Official title
- Feasibility and Clinical Impact Study of Non Pharmacological Interventions Targeting the Subject's Empowerment Among Slackline, Mindfulness, Adapted Physical Activity, Self-hypnosis, Qi Gong Versus Usual Care in Management of Chronic Pain
- Conditions
- Chronic Pain
- Slackline
- Mindfulness
- Adapted Physical Activity
- Self-hypnosis
- Qi Gong
- Interventions
- Other: a systematic proposal for non pharmacological interventions targeting the subject's empowerment among slackline, mindfulness, adapted physical activity, self-hypnosis, and Qi Gong
- Sponsor
- University Hospital, Grenoble
- Collaborators
- Hospices Civils de Lyon; Groupe Hospitalier Mutualiste de Grenoble
- Start date
- 2019-12-18
- Primary completion
- 2023-02-15
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- France
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patient with stable chronic pain defined by the presence of pain for more than 3 months and without substantial change in management in the month prior to inclusion * Patient with a mean EVA maximum daily pain over 7 days greater than or equal to 4/10 * Patient aged 18 and over * Informed and written consent signed by the patient (or his / her legal representative). * Person affiliated with social security or beneficiary of such a scheme Exclusion Criteria: * Patient with a cluster headache * Patient followed for 7 years or more by a pain center * Patient treated with adjuvant or neo-adjuvant chemotherapy or radiotherapy for the primary tumor * Patient with a decompensated psychiatric condition * Patient currently participating or having participated in the month prior to inclusion in another interventional clinical research that may impact the study; this impact is left to the investigator's discretion * Protected persons
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04176341