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Prevention of Pain Induced During Bed Bath in Ehpad

Prevention of Pain Induced During Bed Bath in Ehpad, by Adapted Mobilization Techniques : A Single Case Experimental Design (ABAB) Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07691385
Acronym
TODOMOB
Enrollment
12
Registered
2026-07-08
Start date
2026-07-06
Completion date
2027-11-30
Last updated
2026-07-09

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

Conditions

Geriatric Care

Keywords

Induced pain, Nursing home, personal hygiene, mobility, Non-pharmacological approach

Brief summary

Residents of long-term care facilities are subjected to procedures and treatments that may be painful. The prevalence is 90% among older adults living in institutions. Preventing procedure-induced pain is essential, as the consequences can be even more harmful. Induced pain is defined as "short-term pain caused by a healthcare provider, treatment, or care, under predictable circumstances," according to the UPSA Pain Institute. For these older adults, personal hygiene is performed in bed by nursing assistants and requires frequent handling and repositioning. It includes dressing and undressing, which are sources of pain. Despite this, these activities are repeated daily because they are essential. Addressing pain is a fundamental criterion for quality of life in older adults. In many cases, these residents require daily premedication with analgesics to prevent pain caused by personal care. For these residents, who are already on multiple medications, the addition of analgesics increases the risk of drug interactions, leading to more frequent side effects.

Detailed description

For residents who meet the eligibility criteria, a member of the research team-including the physician and the psychomotor therapist-meets with the resident to inform them about the study and obtain their verbal consent, if possible. If the resident is unable to give consent, the information is provided to the family or a trusted representative by phone or during a visit to the nursing home. The representative may ask the care team any questions and give oral consent after sufficient time to consider the matter. If consent is given, the resident is then enrolled and randomized into the study. Randomization will be based on the number of days in the first week (5, 6, or 7 days) and will be performed by the investigator in the eCRF. The psychomotor therapist will provide expertise that the nursing assistants (NAs) will need to apply during their daily care routines throughout the pilot period in order to make care sessions less unpleasant and painful for the residents.

Interventions

OTHERStandard personal hygiene

Caregivers follow the standard guidelines for personal hygiene. They are not trained by the psychomotor therapist.

OTHERAdapted toilet

Care assistants follow the psychomotor therapist's recommendations for providing appropriate personal care to residents. A new approach to pain prevention developed by a psychomotor therapist and shared with nursing assistants who assist with bedside hygiene for residents experiencing pain of 2 or higher on the ALGOPLUS scale.

Sponsors

Hôpital NOVO
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Inclusion criteria common to all groups * Senior residents * With a stable Algoplus score of 2 or higher * Information provided to and consent obtained from the resident or their trusted representative * Eligible for intervention by a psychomotor therapist Criteria specific to Group 1: * Residents requiring high doses of analgesics (Level 3) before bathing * GIR (Iso-Resource Group) 1, with multiple medical conditions Criteria specific to Group 2: * Residents requiring Level 1 or 2 analgesics before bathing * GIR (Iso-Resource Group) 2 or 3, with multiple medical conditions Criteria specific to Group 3: * Residents experiencing pain without analgesics prior to bathing * GIR (Iso-Resource Group) 3 or 4, with multiple medical conditions

Exclusion criteria

* Resident who has previously received treatment from a psychomotor therapist * Resident capable of washing at the sink (partially) or independently * Under guardianship, conservatorship, or judicial protection

Design outcomes

Primary

MeasureTime frameDescription
Pain reduction with ALGOPLUS4 weeksPain measured using the ALGOPLUS scale by one independent evaluator (an experienced medical or paramedical professional) after bathing.

Secondary

MeasureTime frameDescription
Drug profile4 weeksChange in the dose of pain medication received, by 3 categories of residents
Satisfaction of care workers4 weeksQuestionnaire on changes in practices and how they were perceived, before the study and after each bath
Bathing Process4 weeksNumber of caregivers, duration of care

Countries

France

Contacts

CONTACTVella QUILLIEN
vella.quillien@ght-novo.fr01 30 75 51 75
PRINCIPAL_INVESTIGATORVella QUIILIEN

Hôpital NOVO

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 10, 2026