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Acceptability of an Acupuncture Intervention in Painful Elderly

Acceptability of a Strategy Including Acupuncture in the Treatment of MusculoSkeletal Pain in Hospitalised Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01043692
Acronym
ACUPUNCTURE
Enrollment
60
Registered
2010-01-07
Start date
2007-10-31
Completion date
2008-12-31
Last updated
2013-10-08

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

Conditions

Chronic Pain

Keywords

Chronic Pain > 3 months, Acupuncture, Acceptability, Geriatrics

Brief summary

The aim is to investigate the feasibility and efficacy of an acupuncture intervention on persistent MusculoSkeletar pain in a long-term geriatric hospital care ward population. The main issue is the acceptability of this type of complementary and alternative medicine in older people, although the efficacy on pain is assessed too.

Detailed description

The first 60 patients wanting to participate are enrolled. For the impaired patients, family or legal representing is solicited. The Regional Ethic Committee agreement was granted. The intervention consists in 8 acupuncture sessions. Evaluation * Acceptability : the proportion of patients who complete the whole treatment ; the acceptability at each acupuncture session is recorded. * Pain : Dolorous Scale . The evaluation is based on pre and post treatment variations. As a high proportion of patients have cognitive impairment, the behavioural pain scale dolorous has been chosen after staffs training for all patients, although extra auto evaluation is used when possible (EVS). Evaluation takes place after 5 sessions and after the end of the intervention as well as 2 and 4 weeks after the interventionProfessional carers' satisfaction is recorded.

Interventions

OTHERAcupuncture

Acupuncture in the Treatment of MUSCULOSKELETAR Pain in Hospitalised Elderly

Sponsors

Fondation de France
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* age \> 60 years * chronic musculoskeletal pain * follow up 10 weeks * patient or legal representative's agreement to participate and to the informatics treatment of the data

Exclusion criteria

* acute pain * exclusive neurological pain * coagulation disorders or anticoagulant curative treatment

Design outcomes

Primary

MeasureTime frame
Taux acceptability of the totality of treatment6 months

Secondary

MeasureTime frame
Participation rateevery visit
Motives behind the acceptance or rejectionat Visit 0 to 8
Pain decrease assessment : DOLOPLUS score (observer-assessed evaluation of pain) before/ater intervention, for all the patients Simple descriptive pain intensity scale (VS) (self assessment evaluation of pain) for communicative patientsat Visit 0, 6, 9, 10 and 11
Pain therapeutic's decreaseevery visit
Patient's benefit - Carers satisfaction (questionnaire)at Visit 0,6, 9, 10 and 11

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026