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Study on reducing anxiety and pain during blood donation using hand grip exercise.

To Assess The Effect of Handgrip Compression On Phlebotomy Related Anxiety and Pain- A Randomized Controlled Trial In Whole Blood Donors. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107993
Enrollment
320
Registered
2026-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

None listed

Interventions

Intervention1: Hand Grip Compression Technique: Participants will be instructed to perform hand grip compression using a soft rubber ball during venipuncture and blood donation. Donors will be asked t

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult donors aged 18 to 65 years of either gender eligible for whole blood donation as per department SOP and DCA act 1940, rules and regulation 1945, 2nd amendment 2020 and willing to participate in the study

Exclusion criteria

Exclusion criteria: 1.Donors who are not eligible for whole blood donation as per department SOP and DCA act. 2.Donors with history of adverse effects during any previous donations. 3.Donors who refuse to participate.

Design outcomes

Primary

MeasureTime frame
1.Comparison of mean pre phlebotomy anxiety scores between the intervention group and the control group. 2.Comparison of immediate post venipuncture/phlebotomy pain scores between the two study arms.Timepoint: The outcome in this study will be assessed at procedure specific time points. Anxiety will be assessed immediately prior to phlebotomy, in the blood donation couch. Pain will be assessed shortly after completion of phlebotomy, within a few minutes post procedure.

Secondary

MeasureTime frame
1. Proportion of donors experiencing moderate to severe pain 2. Correlation between anxiety & pain scores Timepoint: The secondary outcomes will be assessed at defined procedural time points a. Proportion of donors experiencing moderate to severe pain will be assessed immediately after completion of phlebotomy. b. Correlation between anxiety & pain scores will be evaluated using anxiety scores recorded immediately prior to phlebotomy & pain scores recorded immediately after phlebotomy.

Countries

India

Contacts

Public ContactDr Suchet Sachdev

Post Graduate Institute of Medical Education and Research

suchet.sachdev@gmail.com9463961690

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026