Robot-Assisted Meditation for Older Adults With Cognitive Concerns

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65-80
SponsorJohns Hopkins University

About this trial

While traditional app-based mindfulness meditation programs relying solely on audio guidance have shown potential benefits for older adults, the apps often face challenges such as low compliance. Participants frequently report difficulties in maintaining focus during meditation sessions, which can limit its effectiveness in improving outcomes such as stress reduction and sleep quality. Recognizing these limitations, this study explores whether a haptic-enabled handheld robot can enhance meditation practices by providing both haptic and audio guidance. The robot, designed to foster sustained attention and encourage rhythmic breathing, may offer a novel, multidimensional approach that addresses compliance issues and supports deeper engagement in mindfulness meditation.

The study primarily seeks to answer the question: Does robot-guided meditation, combining both haptic and audio guidance, improve the sleep quality of older adults living alone with subjective cognitive decline more effectively than traditional audio-based mindfulness meditation guidance? Furthermore, the study examines a secondary question: Is the effect of robot-guided meditation on sleep quality mediated by reductions in stress? By investigating these questions, the research aims to offer insights into whether haptic-enabled meditation technology can overcome common barriers to mindfulness practices among older adults and serve as an innovative tool to improve physical, emotional, and cognitive well-being.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants have subjective cognitive decline, assessed using the Subjective Cognitive Decline Questionnaire (SCD-Q)

Disqualifiers

Participants do not have dementia or mild cognitive impairment.

To exclude significant cognitive impairment, investigators will utilize the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Robot-Guided Meditation

    Behavioral

    A handheld robot provides daily mindfulness meditation sessions that include both haptic and audio guidance.

  • Audio-Guided Control

    Behavioral

    Participants use a standard mindfulness meditation app offering audio-only daily meditation sessions.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Robot-GuidedExperimental treatment 1 intervention
Group B: Audio-GuidedActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Sleep quality as assessed by the Pittsburgh Sleep Quality Index (PSQI)

Pittsburgh Sleep Quality Index (PSQI). The total score range 0 to 21, where a score greater than 5 indicates poor sleep quality. A higher score indicates worse sleep quality.

Time frame
Baseline, 4 weeks, 8 weeks, 12 weeks

Secondary outcomes

1

Stress level as assessed by the Perceived Stress Scale (PSS)

Perceived Stress Scale (PSS). The total score ranges 0 to 40. Low Stress: 0-13; Moderate Stress: 14-26; High Stress: 27-40. A higher score indicates a higher level of perceived stress.

Time frame
Baseline, 4 weeks, 8 weeks, 12 weeks

Other outcomes

1

Adherence

Adherence is defined as the number of days a participant completes the required meditation sessions. Adherence will be tracked through self-reported practice logs and usage data.

Time frame
From enrollment up to end of treatment at 8 weeks

Locations

This trial has no locations.

Sponsors and contacts

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