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Teleconsultations Hypnosis Sessions for Patients with Peripheral Chronic Neuropathic Pain

Monocentric Pilot Study of the Feasibility of Teleconsultations Hypnosis Sessions Led by a Nurse for Patients with Peripheral Chronic Neuropathic Pain - HYPTEC

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05623449
Acronym
HYPTEC
Enrollment
30
Registered
2022-11-21
Start date
2023-02-23
Completion date
2024-04-30
Last updated
2024-11-25

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

Conditions

Peripheral Neuropathy, Pain

Keywords

peripheral chronic neuropathic pain, hypnosis, teleconsultations, feasability

Brief summary

The aim of this study is to assess the feasibility of hypnosis sessions performed in teleconsultations and led by a nurse, for patients with peripheral chronic neuropathic pain. Acceptability, satisfaction and effects (on pain and psychological distress) are also evaluated, comparing patients who have benefited from teleconsultations and those who did not.

Detailed description

Factors explaining peripheral chronic neuropathic pains are complex ; they require a personalized therapeutic strategy and multidisciplinary management. Among the recommended management, psychocorporal approaches such as hypnosis, are subject of recent interest. At the CHU de Bordeaux, the management of patients suffering from such chronic pains, consists of 5 hypnosis sessions, conducted face-to-face, each performed one month apart : the first session is carried out by a doctor and a hypnotherapist nurse and the 4 following sessions by the hypnotherapist nurse alone. However, it seems that this usual management is not easily accessible for patients who are geographically distant and/or who are unable to move due to excessive pain. In such situations, teleconsultations would avoid travel for these patients with low mobility and then would an interesting alternative to face-to-face consultations. Few studies have been done on hypnosis sessions led by teleconsultations. So, the whole purpose of this study is to compare the management of 15 patients by teleconsultations (experimental arm) with 15 other patients seen in face-to-face (control arm) to evaluate feasibility of teleconsultation in hypnosis.

Interventions

OTHERClinical examination

Current medications (only those prescribed to treat pain, anxiety and depression), non-drug treatment(s) prior to treatment in hypnosis as well as any ongoing treatment(s).

OTHERAnxiety and Depression Scale (HAD)

To screen for anxious and depressive symptoms

PROCEDUREpain scale

Measurement of pain intensity

PROCEDUREhypnosis consultation

5 hypnosis consultation

PROCEDUREMaintenance

Qualitative assessment

OTHERData collection

Age, sex, socio-professional category, level of education, comorbidities, date of diagnosis of chronic peripheral neuropathic pain, distance between home and hospital.

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Patient aged over 18 years old, * Patient suffering of from peripheral neuropathic pain for more than 1 year, * Patient referred for hypnosis management as part of a coordinated care support, * Patient who accepts teleconsultation, having the appropriate equipment to attend teleconsultations (computer, microphone, camera and stable internet connection with sufficient internet speed) and the ability to use it independently, * Patient having signed a free, informed and written consent, * Patient affiliated or beneficiary of the social security system.

Exclusion criteria

* Patient with severe and unstable neurocognitive or psychiatric conditions (depression, psychoses, major cognitive impairments), * Patient with uncorrected deafness, * Patient with poor understanding of French * Patient placed under judicial safeguard, guardianship or curatorship.

Design outcomes

Primary

MeasureTime frameDescription
5 hypnosis consultations (in face-to-face and by teleconsultation).Month 8The rate (%) of included patients who have completed the 5 hypnosis consultations (in face-to-face and by teleconsultation).

Secondary

MeasureTime frameDescription
Achievement/AcceptabilityMonth 8Acceptance rate (%) of the proposal to participate in the study in the two study arms: face-to-face hypnosis care (control arm) and care including hypnosis teleconsultations (experimental arm).
Numerical Pain AssessmeDay 0, month 1, month 2, month 3 month 4 and montth 7Mean difference in pain score, minimum value is 0 and maximum value is 10
Hospital Anxiety and Depression scale (HAD)Day 0, month 4 and month 7Mean difference in the anxiety and depression score, minimum value is 0 and maximum value is 42
Learning self-hypnosisDay 0, month 1, month 2, month 3 month 4 and montth 7Evaluate the frequency of the use of self-hypnosis throughout the treatment.
Ssatisfaction scaleMonth 7Evaluate the level of satisfaction and the feeling of the patients with regard to the nursing care in hypnosis at the end of the care in the two study arms (face-to-face control arm and experimental arm with teleconsultations).

Countries

France

Outcome results

None listed

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