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Effect of Guided Imagery on Well-being in Patients With Multiple Sclerosis

Effect of Guided Imagery on Well-being in Patients With Multiple Sclerosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03177655
Acronym
HLGI
Enrollment
20
Registered
2017-06-06
Start date
2012-03-01
Completion date
2017-03-01
Last updated
2017-06-06

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

Conditions

Multiple Sclerosis (MS)

Brief summary

This single-center interventional study quasi-randomly allocated patients to a guided imagery or control intervention (positive journaling). Data were analyzed with treatment allocation masked.

Detailed description

Interventions: Participants were assigned in alternate order to 10 weekly 1-hour sessions Healing Light Guided Imagery or at-home positive journaling; drop-outs were replaced. Intervention Type: Behavioral Multiple sclerosis (MS) is an autoimmune disease that affects the brain and spinal cord (central nervous system). Because nerves in any part of the brain or spinal cord may be damaged, patients with multiple sclerosis can have symptoms in different parts of the body. Many Multiple Sclerosis patients suffer from depression, fatigue and anxiety in addition to physical symptoms. Drugs prescribed for MS have been shown to not improve these comorbid psychological symptoms. Researchers have shown that mindfulness-based training programs can help MS patients, but these therapies are highly resource demanding and taxing for those involved. Healing Light Guided Imagery (HLGI; supplementary materials) is a guided imagery therapy that simulates a self-hypnotic trance state that has been anecdotally shown to improve depression and fatigue in patients with MS in less time and with fewer support resources. The investigators plan to test whether HLGI can increase patient well-being.

Interventions

OTHERGuided Imagery

Guided Imagery meditation

Keeping a journal

Sponsors

University of California, San Diego
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of Relapsing-Remitting Multiple Sclerosis 2. 18-70 years old 3. Able to read and write in English 4. Able to attend sessions at the UC San Diego School of Medicine * Age group: adult * Gender: both * Target enrollment: 20 Participant

Exclusion criteria

1. Severe depression (score of 31 or higher on the BDI) 2. Very high levels of fatigue (above an average of 6 on the FSS) 3. Low levels of mindfulness (below an average score of 2 on the FMI).

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life (MS-QOL-54)Change from baseline at 10 weeksQuality of Life based on Multiple Sclerosis Quality of Life Instrument (MS-QOL-54)

Secondary

MeasureTime frameDescription
Mood (BDI-II)Change from baseline at 10 weeksDepressed mood based on the Beck Depression Inventory II (BDI-II)
Fatigue (FSS)Change from baseline at 10 weeksFatigue levels based on the Fatigue Severity Scale (FSS)

Countries

United States

Outcome results

None listed

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