Hypnosis for Fear of Falling in Older Adults

Rehabilitation Clinical Trial

Official title:

Hypnosis for Fear of Falling in Hospitalized Older Adults? : a Feasibility Randomized Controlled Study.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04726774
• Other study ID #: BASEC 2018-01550
• Secondary ID: SNCTP000003110
• Status: Completed
• Phase: N/A
• Start date: January 17, 2019
• Est. completion date: July 25, 2019

Study information

• Verified date: January 2021
• Source: University Hospital, Geneva
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Fear of falling is associated with numerous negative health outcomes in older adults and can limit rehabilitation. Few treatments are effective in fear of falling. Hypnosis is now recognized as an effective treatment for a variety of conditions, especially anxiety and pain, which can be integrated safely with conventional medicine. Therefore, the objective was to assess the feasibility of a randomized controlled trial to examine whether hypnosis reduces fear of falling in an inpatient geriatric population. In this randomized pilot trial, patients hospitalized in geriatric rehabilitation wards were randomly allocated to either an intervention group (hypnosis plus usual rehabilitation program) or a control group (usual rehabilitation program only). Primary feasibility outcomes were recruitment rate, retention rate, and adherence to the intervention. Secondary outcomes concerned the impact of hypnosis in rehabilitation in fear of falling scores, functional scores, length of stay, and drugs.

Description:

This single-center randomized controlled feasibility trial was conducted in a 296 beds acute care and rehabilitation geriatric hospital of Geneva University Hospitals (Switzerland). After consent, patients were randomized to either the intervention group or the control group. The randomization sequence was computer-generated (ratio 1:1) and concealed until official patient enrolment. All study staff members, including physiotherapists and occupational therapists, were blinded to group allocation, with the exception of the hypnotherapist. All statistical analyses were performed by a blinded statistician. The intervention consisted of two hypnosis sessions of about 30 minutes, weekly provided, by a physician trained in medical hypnosis. Each session was realized as possible during walking, according to the agreement and the physical status of the participant. The intervention was provided in the complement of the usual rehabilitation program. Both the intervention and control groups received the usual rehabilitation program, a multifactorial fall-and-fracture risk-based assessment, and management intervention, which has been shown to be effective in improving physical parameters related to the risk of fall and disability among high-risk oldest-old patients. This program includes intensive physiotherapy for 2 weeks (i.e., focused on walking and enhancing balance exercises in group or individual and group) and patient education on the risk of falling and on prevention of falls. The target sample size was 30 participants (15 participants in each group, pilot study). The study was approved by the State of Geneva's Ethics Committee (2018-01550). All patients provided written informed consent before any study-related procedure. The feasibility of a randomized controlled trial with hypnosis in rehabilitation was assessed by recruitment rate, retention rate, adherence to hypnosis, and adverse events. Fear of falling was assessed by different validated scales. Each scale was completed by each participant three times (week 0 (at baseline): before intervention; week 1 (during intervention): between the two hypnosis sessions; week 2 (at the end of the study): after all interventions), with or without the help of the occupational therapist. Descriptive statistics were reported as mean ± standard deviation or number (percent). The hypnosis and the control groups were compared at baseline using t-tests or Fisher's exact test as appropriate. Longitudinal data were analyzed according to the intention-to-treat concept. Longitudinal data for fear of falling scores, Functional Independence Measure score, and Short Physical Performance Battery score, were analyzed using linear mixed-effects regression models, a negative binomial model for in-hospital falls, and t-tests for medications and length of stay. The incidence of in-hospital falls during hospital stay was analyzed using a negative binomial regression model.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: July 25, 2019
• Est. primary completion date: July 25, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• admitted in a rehabilitation program specialized in falls and fracture risk assessment and management
• 65 years and over

Exclusion Criteria:

• psychiatrics disorders
• did not speak french
• lacking decisional capacity

Related Conditions & MeSH terms

• Fear of Falling
• Older Adults
• Rehabilitation

Intervention

Behavioral:
• Hypnosis
Two sessions of hypnosis, about 30 minutes each, weekly provided, by a physician trained in medical hypnosis. Each session was realized as possible during walking, according to the agreement and the physical status of the participant. Each sessions of hypnosis includes 3 phases : induction, walk perception alteration and post-hypnotic suggestion.
• Rehabilitation program
Intensive physiotherapy for 2 weeks, with walking and balance exercises, (individual and group exercises). Education of risk of falling and prevention of falls.

Locations

Country	Name	City	State
Switzerland	Department of Rehabilitation and Geriatrics, Geneva University Hospitals	Geneva

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of recruitment	recruitement rate was defined by the number of included patients dividing by the number of weeks it takes to include them.	through study completion, an average of 6 months
Primary	feasibility of hypnosis	hypnosis adherence was defined by the number of total sessions of hypnosis	through study completion, an average of 6 months
Secondary	Impact of hypnosis on fear of falling	by comparing scores of questionnaires validated to assess fear of falling between groups	through study completion, an average of 6 months
Secondary	Impact of hypnosis on functional	by comparing functional ability assessed by Functional Independency Measure score and Short Physical Performance Battery score between both groups	through study completion, an average of 6 months
Secondary	Impact of hypnosis on length of stay	length of stay was defined by the number of day of hospitalization, and was compared between both groups	through study completion, an average of 6 months
Secondary	Impact of hypnois on number of drugs	number of drugs at the end of hospitalization	through study completion, an average of 6 months