ClinicalTrials.gg
Status unknownNCT05009147Updated Apr 7, 2022

Home-based Massage by Caregivers for Dementia

An interventional study of Home-based massage by caregivers for dementia in Dementia, Massage and Burden, sponsored by National Taipei University of Nursing and Health Sciences. Status unknown at 1 site in Taiwan. Open to participants aged 65 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-04-07.

Sponsored by National Taipei University of Nursing and Health Sciences · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Jan 2021, registered Aug 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
65 Years and older
Sex
All
01

Study summary

The purpose of this study is to investigate the effects of manual massage on improving behavioral and psychological symptoms of dementia and sense of burden among caregivers.

Read the detailed description

A total of 40 patients with dementia and their family caregivers will be included and randomly allocated to experiment (n=20) or control group (n=20). The experiment and control group will receive whole body manual massage and placebo intervention (30 minutes once per week for 8 continuous weeks), respectively.

02

Conditions studied

  • Dementia
  • Massage
  • Burden

Browse trials for

03

In context

Dementia

2,230 studies on the registry are indexed under Dementia; 549 are open to participants now.

This study's planned enrollment of 40 is below the median of 83 across 1,669 interventional studies indexed under Dementia.

Browse Dementia studies →

Lead sponsor

National Taipei University of Nursing and Health Sciences is the lead sponsor of 123 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Over 65 years old, diagnosed with dementia, agitation or depression, irregular massage and exercise habits.

Exclusion criteria

Exclusion Criteria:

  • Those who have open wounds, inflammation, infection, burns and scalds, artificial blood vessels in the hands, or diagnosed as inappropriate for massage in the near future, the severity of symptoms affects the study participants.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    experimental group

    receive whole body manual massage

    Other: Home-based massage by caregivers for dementia

  • No intervention
    control group

    After experiment, receive whole body manual massage

Interventions

  • OtherHome-based massage by caregivers for dementia

    A total of 40 patients with dementia and their family caregivers will be included and randomly allocated to experiment (n=20) or control group (n=20). The experiment and control group will receive whole body manual massage and placebo intervention (30 minutes once per week for 8 continuous weeks), respectively.

06

What researchers measure

Primary outcomes

  1. change agitation

    Cohen-Mansfield Agitation Inventory (CMAI)

    Time frame: before , during and after 8-weeks massage training interventions

  2. change depression

    Cornell Scale for Depression in Dementia (CSDD)

    Time frame: before , during and after 8-weeks massage training interventions

  3. change stress

    Perceived Stress Scale(PSS)

    Time frame: before , during and after 8-weeks massage training interventions

07

Study locations

1 of 1 sites recruiting
  • National Taipei University of Nursing and Health Sciences
    Taipei, 11219, Taiwan
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2021 (actual). Primary completion is estimated for May 2022, 16 months after the start.

Of 835 non-industry interventional studies with no phase under Dementia, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 43. This study's planned 16 months is below that.

Counting every sponsor, half of 875 studies reached it within 24 months; a quarter within 11 and three quarters within 43.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 8, 2021
First posted
Aug 17, 2021
StartActual
Jan 1, 2021
Primary completionEst.
May 31, 2022
CompletionEst.
May 31, 2022
Last update
Apr 7, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 7, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05009147
Responsible party
CY Song (Prof, National Taipei University of Nursing and Health Sciences) — Principal investigator
First posted
Aug 17, 2021
Start date
Jan 1, 2021
Primary completion
May 31, 2022 (estimated)
Completion
May 31, 2022 (estimated)
Last update
Apr 7, 2022

Study contacts

Chen-Yi Song
Contact
cysong@ntunhs.edu.tw
886-2-28227101 ext. 6136
Chen-Yi Song
principal investigator · National Taipei University of Nursing and Health Sciences

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion