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A Mindful Community for People With ALS and Their Primary Caregivers

A Mindful Community for People With ALS and Their Primary Caregivers

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05595850
Enrollment
100
Registered
2022-10-27
Start date
2020-05-15
Completion date
2025-04-10
Last updated
2026-04-21

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

Conditions

Amyotrophic Lateral Sclerosis, Caregiver Burden

Keywords

Mindfulness, Quality of Life

Brief summary

The psychological impact of ALS on patients and caregivers is high, significantly affecting their quality of life (QOL). Despite this impact, there is not much research about psychological interventions that could reduce psychological distress and improve QOL. The efficacy of mindfulness-based treatments for the improvement of QOL was previously demonstrated by the investigator's group. Despite preliminary positive results, treatment efficacy tends to weaken over time. The investigators believe that a robust solution to maintain efficacy is to maximize the utilization of technology and emerging social platforms, establishing a "mindful community" to promote and continuously reinforce mindfulness. This project's primary aims are 1) to develop a "mindful" online community of people with ALS and their caregivers, and 2) to test its efficacy in QOL improvement. This two-part intervention consists of 1) optimizing the investigator's prior e-learning platform with a three-week program including cognitive exercises, videos and lectures to increase participants' mindfulness; and 2) involving participants in a "mindfulness community" within a social sharing forum. Assessments will be performed before and immediately post-treatment as well as 3- and 6-months post-program comparing subjects undergoing the intervention to a control group.

Interventions

BEHAVIORALMindfulness

Online non-meditation mindfulness program

BEHAVIORALMindful Learning

Online learning program

Sponsors

Harvard University
Lead SponsorOTHER
Catholic University of the Sacred Heart
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Caregiver)

Eligibility

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

Inclusion criteria

For the ALS patients * a definite, probable, laboratory-supported, or possible ALS by revised El-Escorial criteria * they must have the physical ability, with or without adaptive devices, to use a smartphone, a tablet, or a computer * have access to the Internet. For the caregivers * be the person who resides with the ALS patient and is the major provider of unpaid care and assistance (typically, the spouse or another close relative) * s/he must be able to use the application * have access to the Internet.

Exclusion criteria

\- Using shared devices. Patients and caregivers should have their own devices.

Design outcomes

Primary

MeasureTime frameDescription
ALS Specific QOL Short Form Quality of Life (ALSSQOL-SF) - For PALS (Persons with ALS)3 monthsThe ALSSQOL-SF is a 20 item quality of life instrument for patients. It has a 0-10 rating scale with higher scores denoting higher QOL.
World Health Organization Quality of Life (Brief) WHO-QoL BREF - For Caregivers of PALS3 monthsThe WHO-QoL BREF is a 26 item quality of life scale covering four domains of QOL. Each item is scored from 1-5 with higher response employing a higher quality of life. Items are scored from 1-5

Secondary

MeasureTime frameDescription
Hospital Anxiety and Depression Scale (HADS)3 weeks, 3 months, 6 months after joiningThe HADS measures anxiety and depression in a general medical population of patients. It has seven items each for depression and anxiety sub scales. Scoring ranges from 0 to 3, with 3 denoting the highest anxiety or depression level. A total sub scale score of over 8 out of 21 denotes considerable symptoms of either.
Functional Status3 weeks, 3 months, 6 months after joiningSelf-Administered Functional Rating Scale Revised
Zarit Burden Interview3 weeks, 3 months, 6 months after joiningThe ZBI consists of 22 items rated on a 5-point Likert scale that ranges from 0 (never) to 4 (nearly always) with the sum of scores ranging between 0-88. Higher scores indicate greater burden. A score of 17 or more has been considered high burden.
ALS Specific QOL Short Form Quality of Life (ALSSQOL-SF)3 weeks, 3 months, 6 months after joiningThe ALSSQOL-SF is a 20 item quality of life instrument for patients. It has a 0-10 rating scale with higher scores denoting higher QOL.
World Health Organization Quality of Life (Brief) WHO-QoL BREF3 weeks, 3 months, 6 months after joiningThe WHO-QoL BREF is a 16 item quality of life scale covering four domains of QOL. Each item is scored from 1-5 with higher response employing a higher quality of life.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATOREllen Langer, PhD

Harvard University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 22, 2026