Skip to content

Effect of Acupressure on Quality of Life, Sleep Quality, and Hopelessness in Older Adults

The Effect of Acupressure on Quality of Life, Sleep Quality, and Hopelessness in Older Adults: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07435246
Acronym
ACU-ELDER
Enrollment
50
Registered
2026-02-27
Start date
2024-09-01
Completion date
2025-05-30
Last updated
2026-02-27

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

Conditions

Aging, Hopelessness, Sleep Disturbance

Keywords

Acupressure, Older Adults, Sleep Quality, Quality of Life, Hopelessness

Brief summary

This randomized controlled study aims to evaluate the effects of acupressure on quality of life, sleep quality, and hopelessness levels in older adults living in a nursing home setting. Aging is associated with decreased sleep quality, reduced life satisfaction, and increased psychological distress, including hopelessness. Non-pharmacological and low-risk interventions are increasingly needed to improve well-being in older populations. In this study, 50 participants aged 65 years and older were randomly assigned to either an intervention group (acupressure) or a control group (no intervention). The intervention group received acupressure applied to Shenmen (HT7), Neiguan (P6), and Sanyinjiao (SP6) points three times per week for four weeks. The control group received routine care without additional intervention. Outcomes were measured before and after the intervention using the CASP-19 Quality of Life Scale, the Richard-Campbell Sleep Questionnaire, and the Beck Hopelessness Scale. The study evaluates whether acupressure can serve as a safe and effective complementary nursing intervention to improve sleep and overall well-being in older adults.

Detailed description

This randomized controlled trial was conducted to investigate the effect of acupressure on quality of life, sleep quality, and hopelessness among older adults residing in a nursing home. A total of 50 participants aged 65 years and older were included in the study. Participants were randomly assigned to either the intervention group (n=25) or the control group (n=25) using simple randomization. Eligibility criteria included being 65 years or older, residing in the nursing home, and having the ability to read and understand study materials. Individuals with skin lesions, infection, sensory loss in acupressure areas, or those unwilling to participate were excluded. The intervention group received acupressure applied to bilateral Shenmen (HT7), Neiguan (P6), and Sanyinjiao (SP6) points. Each point was stimulated manually for approximately two minutes per session. The intervention was administered three times per week for four consecutive weeks by a trained researcher. The control group received routine institutional care without additional intervention. Primary and secondary outcomes were assessed before and after the intervention. Quality of life was measured using the CASP-19 scale, sleep quality was evaluated using the Richard-Campbell Sleep Questionnaire, and hopelessness levels were measured using the Beck Hopelessness Scale. Data were analyzed using independent-samples t tests and paired-samples t tests. The study aimed to determine whether acupressure could improve sleep quality and quality of life and reduce hopelessness in older adults. This intervention represents a low-cost, non-invasive complementary nursing approach that may support holistic elderly care.

Interventions

OTHERAcupressure

Manual acupressure was applied bilaterally to HT7, P6, and SP6 points. Each point was stimulated for approximately two minutes per session. The intervention was administered three times weekly for four consecutive weeks by a trained researcher.

Sponsors

Kocaeli Sağlık ve Teknoloji Üniversitesi
Lead SponsorOTHER
Kafkas University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The statistician who analyzed the data was blinded to group allocation. Participants were not informed about group assignment during data collection.

Intervention model description

Randomized, parallel-group controlled study with two arms (acupressure intervention and routine care control group). Participants were assigned in a 1:1 ratio.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged 65 years or older * Residing in the nursing home where the study was conducted * Able to communicate verbally * Able to read and understand the questionnaires * Volunteered to participate in the study

Exclusion criteria

* Presence of skin lesions, wounds, or infection at acupressure points * Diagnosed cognitive impairment preventing questionnaire completion * Severe hearing or communication problems * Receiving another complementary therapy during the study period * Refusal to continue participation

Design outcomes

Primary

MeasureTime frameDescription
Change in Sleep Quality ScoreBaseline (Week 0) and Week 4Sleep quality was assessed using the Richard-Campbell Sleep Questionnaire (RCSQ). The total score ranges from 0 to 100, with higher scores indicating better sleep quality. The primary endpoint was the change in total score from baseline to week 4.

Secondary

MeasureTime frameDescription
Change in Quality of Life ScoreBaseline (Week 0) and Week 4Quality of life was measured using the CASP-19 scale. Total scores range from 0 to 57, with higher scores indicating better quality of life. Change from baseline to week 4 was analyzed.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026