ClinicalTrials.gg
Not yet recruitingNCT07904611Updated Oct 29, 2026

Integrating Rhythmical Massage in Palliative Care

An interventional study of Rhythmic Massage in Palliative Care, Health Services, Palliative Care and Massage Intervention, sponsored by Monash University Malaysia. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Monash University Malaysia · Not applicable, Interventional, and Supportive care

Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

People receiving palliative and end-of-life care may experience pain, fatigue, sleep difficulties, anxiety, and other symptoms that affect their comfort and quality of life. While standard medical treatments are important, additional supportive approaches may help promote comfort and wellbeing.

Rhythmical Massage (RM) is a gentle, non-invasive touch-based approach involving rhythmic movements, light touch, warmth, and rest. However, there is limited evidence on its use in palliative care in Malaysia.

This research will evaluate RM using quantitative measures of symptom burden, pain intensity, sleep quality, and physiological responses among people receiving palliative and end-of-life care in a community hospice. RM will be provided alongside, and will not replace, usual medical and palliative care. The findings will provide locally relevant evidence on the potential benefits, safety, experiences, and practical considerations of using RM as a complementary supportive approach in Malaysian palliative care.

02

Conditions studied

  • Palliative Care, Health Services
  • Palliative Care
  • Massage Intervention

Keywords

  • Rhythmical massage
  • Palliative care
  • End-of-Life Care
03

In context

Lead sponsor

Monash University Malaysia is the lead sponsor of 14 studies on the registry; 6 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Individuals receiving palliative or end-of-life care at a participating community hospice.
  • Individuals clinically appropriate to receive Rhythmical Massage (RM), as determined by the treating healthcare professional.
  • Individuals able to read and understand the study information and provide written .

Exclusion criteria

Exclusion Criteria:

  • Individuals whose clinical condition or other circumstances make receiving RM inappropriate or potentially cause undue discomfort, as assessed by the treating healthcare professional and RM practitioner.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Adults receiving palliative or end-of-life care at a community hospice

    Other: Rhythmic Massage

Interventions

  • OtherRhythmic Massage

    Rhythmical Massage (RM) is a gentle, non-invasive, touch-based approach involving rhythmic movements, light pressure, warmth, and a period of rest following each session. In this study, participants will receive approximately 4-6 RM sessions over 2-3 weeks, administered by trained RM practitioners.

06

What researchers measure

Primary outcomes

  1. Change in Symptom Burden

    Change in symptom burden measured using the Edmonton Symptom Assessment System (ESAS), which assesses the severity of symptoms experienced by people receiving palliative care.

    Time frame: Baseline (before the first RM session) to the end of the intervention period (approximately 2-3 weeks).

  2. Change in Pain Intensity

    Change in pain intensity measured using a Visual Analogue Scale (VAS), with participants rating their pain intensity on a scale from 0 (no pain) to 10 (worst imaginable pain).

    Time frame: Before and immediately after each Rhythmical Massage (RM) session, across approximately 4-6 sessions over 2-3 weeks.

Secondary outcomes

  1. Change in Sleep Quality

    Change in sleep quality measured using the Pittsburgh Sleep Quality Index (PSQI), which assesses sleep quality and sleep disturbances.

    Time frame: Baseline to the end of the intervention period (approximately 2-3 weeks).

  2. Change in Heart Rate Variability (HRV)

    Changes in heart rate variability, including high-frequency (HF) power and the standard deviation of normal-to-normal intervals (SDNN), measured to assess changes in autonomic cardiac activity associated with Rhythmical Massage (RM).

    Time frame: Immediately before and after each RM session, across approximately 4-6 sessions over 2-3 weeks.

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Walchli C, Saltzwedel G, Kruerke D, Kaufmann C, Schnorr B, Rist L, Eberhard J, Decker M, Simoes-Wust AP. Physiologic effects of rhythmical massage: a prospective exploratory cohort study. J Altern Complement Med. 2014 Jun;20(6):507-15. doi: 10.1089/acm.2012.0833. Epub 2013 May 23. PubMed 23700977 ↗
  • Werthmann PG, Cysarz D, Jungbluth M, Lederer AK, Nenova G, Huber R, van Dijk M, Kienle GS. Efficacy and safety of massage for postoperative stress in colorectal cancer patients: a randomized, controlled, three-arm trial. Front Oncol. 2025 Feb 5;15:1439420. doi: 10.3389/fonc.2025.1439420. eCollection 2025. PubMed 39980553 ↗

Individual participant data

Plan to share: No — Upon request via direct contact to researcher

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Feb 2027; primary completion for Aug 2028, 18 months later.

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

Registered
Oct 23, 2026
First posted
Oct 29, 2026
StartEst.
Feb 1, 2027
Primary completionEst.
Aug 31, 2028
CompletionEst.
Dec 31, 2028
Last update
Oct 29, 2026
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.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07904611
Lead sponsor
Monash University Malaysia
Responsible party
Teoh Siew Li (Senior Lecturer, School of Pharmacy, Monash University Malaysia, Monash University Malaysia) — Principal investigator
First posted
Oct 29, 2026
Start date
Feb 1, 2027 (estimated)
Primary completion
Aug 31, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Oct 29, 2026

Study contacts

Siew Li Teoh
Contact
teoh.siew.li@monash.edu
+6012-3223273

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 not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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