Evaluating the Effectiveness of Osteopathy in the Management of Pain in Elderly People

Evaluating the Effectiveness of Osteopathy in the Management of Pain in Elderly People in Residential Care Facilities for the Elderly (EHPAD)

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03382236

Acronym

IPODE

Enrollment

Registered

2017-12-22

Start date

2017-01-03

Completion date

2018-12-31

Last updated

2017-12-22

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

Conditions

Osteopathy

Brief summary

This type of study can have an impact on public health policy and help improve the management of pain in people with EHPAD; Propose better use of drug treatments and non-pharmacological methods such as osteopathy; Help structuring the healthcare sector.

Detailed description

* Osteopathy group: 3 osteopathy sessions of 45 min with one session every 3 weeks at S2, S5 and S8. Fascial osteopathic techniques performed will consist of gentle and non-impulsive manipulation * Simulated group: 3 simulated osteopathy sessions lasting 45 minutes, one session every 3 weeks at S2, S5 and S8. The techniques performed will consist of an application of the hands to different anatomical regions than the group osteopathy without therapeutic intention, that is to say without tissue tensioning. The pain will be assessed at inclusion (S0) and at the end of the procedure (S12) by the head physician, the coordinating physician or the psychomotor therapist, ignoring the assignment group of the subject and before each session. osteopathy (at S2, S5 and S8) by a nurse or psychomotor also ignoring the patient's assignment group. Both groups will continue to benefit from their usual allopathic management and recommendations. Patients will not be aware of the treatment received (osteopathy or simulated) and will be randomized by a computer server.

Interventions

OTHERosteopathy

osteopathic techniques

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

75 Years to No maximum

Healthy volunteers

Inclusion criteria

* Patients older than 75 years * Patients Residing in Accommodation Facilities for Dependent Old People * A score measured by the DOLOPLUS 2 Scale at least 7/30 at the start of the study * For patients in capacity and autonomous: Patients informed and having signed a free and informed consent. For non-capable patients with a trusted person and / or guardian: Informed patients whose confidant or guardian has been informed and has signed free and informed consent. \- Affiliated to a social security scheme (beneficiary or beneficiary)

Exclusion criteria

* Absence of pain * Medical contraindication known to the practice of osteopathy with fascial aim (advanced degenerative bone disease, metastatic cancer) * Osteopathic treatment in the last six months * Patients under curators

Design outcomes

Primary

Measure	Time frame	Description
DOLOPLUS 2 score	Every week after inclusion during 4 weeks	Assessment of pain assessed by the behavioral scale

Countries

France

Outcome results

None listed

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